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Paper · 4045950

A population study of adult onset limb-girdle muscular dystrophy.

Yates JR and 1 other. J Med Genet, 1985. Cited by 33 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. A population study of adult onset limb-girdle muscular dystrophy. Papers, record 4045950. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/4045950

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Paper

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

Title
A population study of adult onset limb-girdle muscular dystrophy.
PubMed
Journal
J Med Genet
PubMed
Year
1985
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
33
iCite
Relative citation ratio, by iCite
1.09
iCite
Revised in PubMed
2019-05-03
PubMed

Authors2

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

OrderAuthorForenameKindORCID iD
1Yates JRJ R
2Emery AEA E

Source PubMed

Topics10

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

MeSH termMajor
Muscular DystrophiesMajor topic
Adolescent
Adult
Creatine Kinase
Electromyography
Female
Humans
Male
Middle Aged
Scotland

Source PubMed

Grants0

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.

None in this release.

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.

References6

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

OrderPMIDTitleJournalYearIn PapersSource
1641,943Unusual inheritance of Becker type muscular dystrophy.J Med Genet1978https://conductscience.org/library/papers/641943PubMed
25,983,007[Progressive muscular dystrophy. 8. Incidence, clinical aspects and genetics of types I and II].Schweiz Med Wochenschr1966https://conductscience.org/library/papers/5983007PubMed
34,854,942The manifesting carrier in Duchenne muscular dystrophy.Clin Genet1974https://conductscience.org/library/papers/4854942PubMed
514,424,475Formal genetics of muscular dystrophy.Am J Hum Genet1959https://conductscience.org/library/papers/14424475PubMed
76,978,204Prevalence and incidence of muscular dystrophy in Alberta, Canada.Clin Genet1982https://conductscience.org/library/papers/6978204PubMed
81,142,377The detection of carriers of benign (Becker-type) X-linked muscular dystrophy.J Med Genet1975https://conductscience.org/library/papers/1142377PubMed

Cited by9

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 33 citations.

PMIDTitleJournalYearIn PapersSource
31,791,368Epidemiological study and genetic characterization of inherited muscle diseases in a northern Spanish region.Orphanet J Rare Dis2019https://conductscience.org/library/papers/31791368PubMed
28,634,560Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma Developed in a Patient with Progressive Muscular Dystrophy: A Case Report and Review of the Literature.Case Rep Orthop2017https://conductscience.org/library/papers/28634560PubMed
27,142,102Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies.BMC Musculoskelet Disord2016https://conductscience.org/library/papers/27142102PubMed
24,024,053Dupuytren's Contracture Cosegregation with Limb-Girdle Muscle Dystrophy.Case Rep Neurol Med2013https://conductscience.org/library/papers/24024053PubMed
18,974,005Calpain 3, the "gatekeeper" of proper sarcomere assembly, turnover and maintenance.Neuromuscul Disord2008https://conductscience.org/library/papers/18974005PubMed
9,973,293Identification of a new autosomal dominant limb-girdle muscular dystrophy locus on chromosome 7.Am J Hum Genet1999https://conductscience.org/library/papers/9973293PubMed
8,556,875Limb girdle muscular dystrophy: a radiologic and manometric study of the pharynx and esophagus.Dysphagia1996https://conductscience.org/library/papers/8556875PubMed
8,533,766Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.Am J Hum Genet1995https://conductscience.org/library/papers/8533766PubMed
8,153,942Lung and respiratory muscle function in limb girdle muscular dystrophy.Thorax1994https://conductscience.org/library/papers/8153942PubMed

Genes0

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

None in this release.

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

Sources 11

  • 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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