Mutation screening of the USH2A gene reveals two novel pathogenic variants in Chinese patients causing simplex usher syndrome 2

BACKGROUND: Usher syndrome (USH) is the most prevalent cause of the human genetic deafness and blindness. USH type II (USH2) is the most common form of USH, and USH2A is the major pathogenic gene for USH2. For expanding the spectrum of USH2A mutations and further revealing the role of USH2A in USH2,...

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Detalles Bibliográficos
Autores principales: He, Chenhao, Liu, Xinyu, Zhong, Zilin, Chen, Jianjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038606/
https://www.ncbi.nlm.nih.gov/pubmed/32093671
http://dx.doi.org/10.1186/s12886-020-01342-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038606/
https://www.ncbi.nlm.nih.gov/pubmed/32093671
http://dx.doi.org/10.1186/s12886-020-01342-y

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