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...

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Bibliografski detalji
Glavni autori: Jaber, L, Shohat, M, Bu, X, Fischel-Ghodsian, N, Yang, H Y, Wang, S J, Rotter, J I
Format: Artigo
Jezik:Inglês
Izdano: 1992
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015845/
https://ncbi.nlm.nih.gov/pubmed/1613771
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