(Q1531320)
English
autosomal dominant limb-girdle muscular dystrophy type 1B
autosomal dominant limb-girdle muscular dystrophy that has material basis in mutation in the gene encoding lamin A/C (LMNA)
- LGMD1B
- Limb-girdle muscular dystrophy due to lamin A/C deficiency
- muscular dystrophy, limb-girdle type 1B
- proximal muscular dystrophy type 1B
- Muscular Dystrophy, Proximal, Type 1B
- Limb-girdle muscular dystrophy type 1B
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B; LGMD1B
- MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B
- obsolete autosomal dominant limb-girdle muscular dystrophy type 1B
Statements
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Identifiers
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Sitelinks
Wikipedia(1 entry)
- dewiki Gliedergürteldystrophie 1B