期刊
HEARING RESEARCH
卷 288, 期 1-2, 页码 89-99出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.heares.2011.12.003
关键词
-
资金
- NIDCD [DC004568, DC000039-15]
Hereditary deafness is genetically heterogeneous such that mutations of many different genes can cause hearing loss. This review focuses on the evidence and implications that several of these deafness genes encode actin-interacting proteins or actin itself. There is a growing appreciation of the contribution of the actin interactome in stereocilia development, maintenance, mechanotransduction and malfunction of the auditory system. Published by Elsevier B.V.
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