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High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing

OBJECTIVE: This study aimed to explore the genetic causes of probands who were diagnosed with Waardenburg syndrome (WS) or congenital sensorineural hearing loss. METHODS: A detailed physical and audiological examinations were carried out to make an accurate diagnosis of 14 patients from seven unrela...

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Detalles Bibliográficos
Autores principales:	Zhang, Sen, Xu, Hongen, Tian, Yongan, Liu, Danhua, Hou, Xinyue, Zeng, Beiping, Chen, Bei, Liu, Huanfei, Li, Ruijun, Li, Xiaohua, Zuo, Bin, Tang, Ryan, Tang, Wenxue
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8212959/ https://www.ncbi.nlm.nih.gov/pubmed/34149797 http://dx.doi.org/10.3389/fgene.2021.643546

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