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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Dades bibliogràfiques
Publicat a:Front Genet
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2021
Matèries:
Genetics
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8212959/
https://ncbi.nlm.nih.gov/pubmed/34149797
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2021.643546
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