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Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99.

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  • Affiliation of Author(s):基础医学院

  • Journal:Hum Mutat

  • All the Authors:shaochangshun,Liu,lijiangxia,jiangbaichun

  • First Author:gongyaoqin

  • Indexed by:Unit Twenty Basic Research

  • Document Code:lw-169865

  • Volume:36

  • Issue:1

  • Page Number:98

  • Translation or Not:no

  • Date of Publication:2015-01-01

  • Date of Publication:2015-01-01
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