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

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    • Institution:基础医学院

    • Title of Paper: Whole-exome Sequencing Identifies a Variant in TMEM132E Causing Autosomal-Recessive Nonsyndromic Hearing Loss DFNB99.

    • Journal:Hum Mutat

    • First Author:龚瑶琴

    • All the Authors:邵常顺,刘奇迹,李江夏,蒋百春

    • Document Code:lw-169865

    • Volume:36

    • Issue:1

    • Page Number:98

    • Translation or Not:No

    • Date of Publication:2015-01

    • Release Time:2019-04-13
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