A carregar...
Sensorineural deafness inherited as a tissue specific mitochondrial disorder.
We present here a large Israeli-Arab kindred with hereditary deafness. In this family 55 deaf subjects (29M, 26F), who are otherwise healthy, have been identified and traced back five generations to one common female ancestor. The deafness is progressive in nature, usually presenting in infancy and...
Na minha lista:
| Publicado no: | J Med Genet |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1992
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015845/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1613771/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.29.2.86 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|