Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in Zebrafish

Hearing loss is one of the most prevalent human birth defects. Genetic factors contribute to the pathogenesis of deafness. It is estimated that one-third of deafness genes have already been identified. The current work is an attempt to find novel genes relevant to hearing loss using guilt-by-profili...

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Detalles Bibliográficos
Autores principales: Liu, Fei, Xia, Wenjun, Hu, Jiongjiong, Wang, Yingzhi, Yang, Fan, Sun, Shaoyang, Zhang, Jin, Jiang, Nan, Wang, Huijun, Tian, Weidong, Wang, Xu, Ma, Duan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573323/
https://www.ncbi.nlm.nih.gov/pubmed/26375458
http://dx.doi.org/10.1371/journal.pone.0136832

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