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Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99

Jiangxia Li1, Xiaohan Zhao, Qian Xin

  • 1Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, Shandong University School of Medicine, Jinan, Shandong, 250012, China.

Human Mutation
|October 22, 2014
PubMed

Keywords:
ARNSHLDFNB99TMEM132Einner hair cellwhole-exome sequencing

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