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Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families

Yingjie Zhou1, Muhammad Tariq2, Sijie He3,4

  • 1Seven Section of Department of Gynaecology, The Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.

BMC Medical Genetics
|July 20, 2020
PubMed
Abstract

Keywords:
Clinical detectionConsanguineous pedigreesHearing lossWhole exome sequencing

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