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Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene?
A family study was carried out to clarify the problem of two separate muscle disease phenotypes in a large consanguineous pedigree. These were a severe limb-girdle type muscular dystrophy and a mild late onset distal myopathy. Thirty-two first degree and 14 other relatives of 18 previously examined...
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
1992
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1015987/ https://ncbi.nlm.nih.gov/pubmed/1619633 |
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