ロード中...
A study of whirlin isoforms in the mouse vestibular system suggests potential vestibular dysfunction in DFNB31-deficient patients
The DFNB31 gene plays an indispensable role in the cochlea and retina. Mutations in this gene disrupt its various isoforms and lead to non-syndromic deafness, blindness and deaf-blindness. However, the known expression of Dfnb31, the mouse ortholog of DFNB31, in vestibular organs and the potential v...
保存先:
| 出版年: | Hum Mol Genet |
|---|---|
| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2015
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4654056/ https://ncbi.nlm.nih.gov/pubmed/26420843 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv403 |
| 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!
|