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A Novel PAX3 Mutation in a Chinese Family with Waardenburg Syndrome Type 1.
Genetic Testing and Molecular Biomarkers ( IF 1.1 ) Pub Date : 2020-05-07 , DOI: 10.1089/gtmb.2019.0231 Shuling Li 1 , Min Guo 1 , Biao Ruan 1 , Ya Liu 1 , Xin Cui 1 , Weiwei Han 1 , Ruomei Li 1
Genetic Testing and Molecular Biomarkers ( IF 1.1 ) Pub Date : 2020-05-07 , DOI: 10.1089/gtmb.2019.0231 Shuling Li 1 , Min Guo 1 , Biao Ruan 1 , Ya Liu 1 , Xin Cui 1 , Weiwei Han 1 , Ruomei Li 1
Affiliation
Aims: To determine the clinical characteristics and genetic cause of Waardenburg syndrome type 1 (WS1) in a Chinese family.
更新日期：2020-05-07
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