A novel PAX3 mutation in a Chinese Han family with Waardenburg syndrome type 1-MedSci.cn

A novel PAX3 mutation in a Chinese Han family with Waardenburg syndrome type 1

Guo, M; Li, Q; Jiang, CW; Li, SL; Ruan, BA

Li, SL; Ruan, BA (corresponding author), Kunming Med Univ, Otorhinolaryngol Dept, Affilliated Hosp 1, 295 Xichang Rd, Kunming 650032, Yunnan, Peoples R China.

INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY, 2021; 147 ():

Abstract

Objectives: To determine the clinical characteristics and genetic causes of Waardenburg syndrome type 1 (WS1) present in a Chinese Han family. Methods......

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