A gene for autosomal recessive limb-girdle muscular dystrophy in Manitoba Hutterites maps to chromosome region 9q31-q33: evidence for another limb-girdle muscular dystrophy locus.

Characterized by proximal muscle weakness and wasting, limb-girdle muscular dystrophies (LGMDs) are a heterogeneous group of clinical disorders. Previous reports have documented either autosomal dominant or autosomal recessive modes of inheritance, with genetic linkage studies providing evidence for...

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Detalhes bibliográficos
Main Authors: Weiler, T, Greenberg, C R, Zelinski, T, Nylen, E, Coghlan, G, Crumley, M J, Fujiwara, T M, Morgan, K, Wrogemann, K
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1377246/
https://ncbi.nlm.nih.gov/pubmed/9634523
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