Characterization of UMi028-A-1 stem cell line that contains a CRISPR/Cas9 induced hearing loss-associated variant (V60L (c.178G > T)) in the P2RX2 gene

Author:

Gosstola Nicholas C.,Huang Zaohua,Tong Xiaoying,Nourbakhsh Aida,Chen Zheng-Yi,Dykxhoorn Derek M.,Zhong Liu Xue

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,General Medicine

Reference3 articles.

1. Progressive dominant hearing loss (autosomal dominant deafness-41) and P2RX2 gene mutations: A Phenotype-Genotype Study;Liu;Laryngoscope,2019

2. Characterization of ATPase activity of P2RX2 cation channel;Rahul;Front. Physiol.,2016

3. Mutation of the ATP-Gated P2X2 Receptor Leads to Progressive Hearing Loss and Increased Susceptibility to Noise;Yan;Proc. National Acad. Sci.,2013

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