Autosomal recessive oculopharyngeal muscular dystrophy.
Oculopharyngeal muscular dystrophy is known as a rare automsomal dominant disease. A family is reported suggesting that there may be genetic heterogeneity in oculopharyngeal muscular dystrophy and that in some families the mode of inheritance may be autosomal recessive. IMAGES:
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| Publicado no: | J Med Genet |
|---|---|
| Principais autores: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1975
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1013325/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1219124/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.12.4.416 |
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