Author:
Zhang Hongfeng,Zhu Lin,Wang Fengpeng,Wang Ruimin,Hong Yujuan,Chen Yangqin,Zhu Bin,Gao Yue,Luo Hong,Zhang Xian,Sun Hao,Zhou Ying,Yao Yi,Wang Xin
Subject
Genetics (clinical),Genetics,Molecular Medicine
Reference31 articles.
1. Founder mutation in KCNJ10 in Pakistani patients with EAST syndrome;Abdelhadi;Mol. Genet. Genomic Med.,2016
2. A method and server for predicting damaging missense mutations;Adzhubei;Nat. Methods,2010
3. Novel mutation in the KCNJ10 gene in three siblings with seizures, ataxia and no electrolyte abnormalities;Al Dhaibani;J. Neurogenet.,2018
4. Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations;Bockenhauer;N. Engl. J. Med.,2009
5. The role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss;Chen;Neuroscience,2014
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