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Paper · 15316618

[Limb girdle muscular dystrophies].

Finsterer J. Nervenarzt, 2004. Cited by 3 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. [Limb girdle muscular dystrophies]. Papers, record 15316618. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/15316618

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Paper

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

Title
[Limb girdle muscular dystrophies].
PubMed
Journal
Nervenarzt
PubMed
Year
2004
PubMed
Publication types
English Abstract, Journal Article, Review
PubMed
Citations, by iCite
3
iCite
Relative citation ratio, by iCite
0.07
iCite
Revised in PubMed
2018-11-13
PubMed

Authors1

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

OrderAuthorForenameKindORCID iD
1Finsterer JJ

Source PubMed

Topics4

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

MeSH termMajor
Genetic Predisposition to DiseaseMajor topic
Muscle ProteinsMajor topic
Muscular Dystrophies, Limb-GirdleMajor topic
Humans

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.

References101

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

OrderPMIDTitleJournalYearIn PapersSource
110,496,277Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy.Neurology1999https://conductscience.org/library/papers/10496277PubMed
212,587,341[Dysferlinopathy. Example of a new myopathy].Bull Acad Natl Med2002https://conductscience.org/library/papers/12587341PubMed
37,663,518Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli.Nat Genet1995https://conductscience.org/library/papers/7663518PubMed
48,533,766Evidence for locus heterogeneity in autosomal dominant limb-girdle muscular dystrophy.Am J Hum Genet1995https://conductscience.org/library/papers/8533766PubMed
510,464,299Phenotypic behavior of caveolin-3 mutations that cause autosomal dominant limb girdle muscular dystrophy (LGMD-1C). Retention of LGMD-1C caveolin-3 mutants within the golgi complex.J Biol Chem1999https://conductscience.org/library/papers/10464299PubMed
68,499,908Exclusion of the 15q locus as a candidate gene for severe childhood autosomal recessive Duchenne-like muscular dystrophy in Brazilian families.Hum Mol Genet1993https://conductscience.org/library/papers/8499908PubMed
714,960,875Screening for C283Y gamma-sarcoglycan mutation in a high-risk group of Bulgarian Gypsies: evidence for a geographical localization and a non-random distribution among Gypsy subgroups.Community Genet2002https://conductscience.org/library/papers/14960875PubMed
814,523,375Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutation.Eur J Hum Genet2004https://conductscience.org/library/papers/14523375PubMed
910,766,988Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation.Am J Med Genet2000https://conductscience.org/library/papers/10766988PubMed
1011,562,567The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more.Curr Opin Neurol2001https://conductscience.org/library/papers/11562567PubMed

1 to 10 of 101

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Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 3 citations.

None in this release.

Genes14

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

GeneNCBI Gene IDLinked byIn GenesSource
CAPN3825PubTator's text mininghttps://conductscience.org/library/genes/825NCBI Gene
CAV3859PubTator's text mininghttps://conductscience.org/library/genes/859NCBI Gene
CBLL2158,506PubTator's text mininghttps://conductscience.org/library/genes/158506NCBI Gene
DYSF8,291PubTator's text mininghttps://conductscience.org/library/genes/8291NCBI Gene
FKRP79,147PubTator's text mininghttps://conductscience.org/library/genes/79147NCBI Gene
LMNA4,000PubTator's text mininghttps://conductscience.org/library/genes/4000NCBI Gene
MYOT9,499PubTator's text mininghttps://conductscience.org/library/genes/9499NCBI Gene
SGCA6,442PubTator's text mininghttps://conductscience.org/library/genes/6442NCBI Gene
SGCB6,443PubTator's text mininghttps://conductscience.org/library/genes/6443NCBI Gene
SGCD6,444PubTator's text mininghttps://conductscience.org/library/genes/6444NCBI Gene

1 to 10 of 14

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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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