Paper · 8533766

Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.

Speer MC and 9 others. Am J Hum Genet, 1995. Cited by 22 papers, by iCite.

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ConductScience Library. Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy. Papers, record 8533766. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/8533766

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.; PubMed
Journal: Am J Hum Genet; PubMed
Year: 1995; PubMed
Publication types: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/8533766/; PubMed
PMC: https://pmc.ncbi.nlm.nih.gov/articles/PMC1801402/; PubMed
The journal: https://conductscience.org/library/journal-index/0370475; PubMed
Citations, by iCite: 22; iCite
Relative citation ratio, by iCite: 0.48; iCite
Revised in PubMed: 2020-08-24; PubMed

Authors10

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename
1	Speer MC	M C
2	Gilchrist JM	J M
3	Chutkow JG	J G
4	McMichael R	R
5	Westbrook CA	C A
6	Stajich JM	J M
7	Jorgenson EM	E M
8	Gaskell PC	P C
9	Rosi BL	B L
10	Ramesar R	R

Source PubMed

Topics12

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
Genetic Heterogeneity	Major topic
Muscular Dystrophies	Major topic
Adolescent
Adult
Age of Onset
Female
Genetic Linkage
Haplotypes
Humans
Male
Middle Aged
Pedigree

Source PubMed

Grants2

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes it	Agency	Country	NIH project	Stated by	Source
CA40046	NCI NIH HHS	United States	P01CA040046	PubMed and NIH	NIH RePORTER
NS26630	NINDS NIH HHS	United States	P01NS026630	PubMed and NIH	NIH RePORTER

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References27

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

Order	PMID	Title	Journal	Year	In Papers	Source
1	8,276,417	Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 region.	Genomics	1993	https://conductscience.org/library/papers/8276417	PubMed
2	8,252,041	Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q.	Nat Genet	1993	https://conductscience.org/library/papers/8252041	PubMed
3	8,056,435	Avoiding recomputation in linkage analysis.	Hum Hered	1994	https://conductscience.org/library/papers/8056435	PubMed
4	8,069,911	Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy.	Cell	1994	https://conductscience.org/library/papers/8069911	PubMed
5	7,825,577	Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q.	Am J Hum Genet	1995	https://conductscience.org/library/papers/7825577	PubMed
6	7,833,913	Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.	Hum Mol Genet	1994	https://conductscience.org/library/papers/7833913	PubMed
7	7,881,291	Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9.	Neuromuscul Disord	1994	https://conductscience.org/library/papers/7881291	PubMed
8	14,424,475	Formal genetics of muscular dystrophy.	Am J Hum Genet	1959	https://conductscience.org/library/papers/14424475	PubMed
9	5,637,795	Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.	Pediatrics	1968	https://conductscience.org/library/papers/5637795	PubMed
10	5,780,363	Genetic studies of a family with two unusual autosomal dominant conditions: muscular dystrophy and Pelger-Huet anomaly. Clinical, pathologic and linkage considerations.	Am J Med	1969	https://conductscience.org/library/papers/5780363	PubMed

1 to 10 of 27

See all 27 references

Cited by8

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 22 citations.

PMID	Title	Journal	Year	In Papers	Source
30,838,352	LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation.	Acta Myol	2018	https://conductscience.org/library/papers/30838352	PubMed
27,747,217	DNAJB6 Myopathies: Focused Review on an Emerging and Expanding Group of Myopathies.	Front Mol Biosci	2016	https://conductscience.org/library/papers/27747217	PubMed
22,366,786	Mutations affecting the cytoplasmic functions of the co-chaperone DNAJB6 cause limb-girdle muscular dystrophy.	Nat Genet	2012	https://conductscience.org/library/papers/22366786	PubMed
15,316,618	[Limb girdle muscular dystrophies].	Nervenarzt	2004	https://conductscience.org/library/papers/15316618	PubMed
9,973,293	Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.	Am J Hum Genet	1999	https://conductscience.org/library/papers/9973293	PubMed
9,634,523	A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.	Am J Hum Genet	1998	https://conductscience.org/library/papers/9634523	PubMed
9,106,535	Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.	Am J Hum Genet	1997	https://conductscience.org/library/papers/9106535	PubMed
8,808,603	Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.	Am J Hum Genet	1996	https://conductscience.org/library/papers/8808603	PubMed

Genes1

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Gene	NCBI Gene ID	Linked by	In Genes
IL9	3,578	PubTator's text mining	https://conductscience.org/library/genes/3578

Source NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

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ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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