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FSHMD1B facioscapulohumeral muscular dystrophy 1B [ Homo sapiens (human) ]

Gene ID: 2490, updated on 2-Oct-2019

Summary

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Gene symbol
FSHMD1B
Gene description
facioscapulohumeral muscular dystrophy 1B
Primary source
MIM:158901
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FSHD1B

Bibliography

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Related articles in PubMed

  1. Further exclusion of FSHD1B from the telomeric region of 10q. Speer MC, et al. Neurogenetics, 1997 Sep. PMID 10732819
  2. Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD). Gilbert JR, et al. Am J Hum Genet, 1993 Aug. PMID 8328457, Free PMC Article
  3. Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD). Cacurri S, et al. Hum Genet, 1994 Oct. PMID 7927331

GeneRIFs: Gene References Into Functions

Phenotypes

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facioscapulohumeral muscular dystrophy 1B

General gene information

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Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases