Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population
Hereditary hearing loss is characterized by a high degree of genetic heterogeneity. Mutations in the TMPRSS3 (transmembrane protease, serine 3) gene cause prelingual (DFNB10) or postlingual (DFNB8) deafness. In our previous study, three pathogenic mutations in TMPRSS3 were identified in one Chinese...
Ausführliche Beschreibung
Bibliographische Detailangaben
| Veröffentlicht in: | Neural plasticity. - 1998. - 2017(2017) vom: 01., Seite 3192090
|
|---|
| 1. Verfasser: |
Gao, Xue
(VerfasserIn) |
|---|
| Weitere Verfasser: |
Huang, Sha-Sha,
Yuan, Yong-Yi,
Xu, Jin-Cao,
Gu, Ping,
Bai, Dan,
Kang, Dong-Yang,
Han, Ming-Yu,
Wang, Guo-Jian,
Zhang, Mei-Guang,
Li, Jia,
Dai, Pu |
|---|
| Format: | Online-Aufsatz
|
|---|
| Sprache: | English |
|---|
| Veröffentlicht: |
2017
|
|---|
| Zugriff auf das übergeordnete Werk: | Neural plasticity
|
|---|
| Schlagworte: | Journal Article
Membrane Proteins
Neoplasm Proteins
Serine Endopeptidases
EC 3.4.21.-
TMPRSS3 protein, human |
|---|