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LGMD1F limb girdle muscular dystrophy 1F (autosomal dominant) [ Homo sapiens (human) ]

Gene ID: 404679, discontinued on 4-Feb-2014

Summary

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Official Symbol
LGMD1Fprovided by HGNC
Official Full Name
limb girdle muscular dystrophy 1F (autosomal dominant)provided by HGNC
Primary source
HGNC:HGNC:33443
See related
MIM:608423
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
7q32.1-q32.2

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
limb girdle muscular dystrophy 1F (autosomal dominant)
GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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