ロード中...
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...
保存先:
| 出版年: | J Med Genet |
|---|---|
| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BMJ Publishing Group
1992
|
| 主題: | |
| オンライン･アクセス: | 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 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|