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KCNJ10 gene

Known as: KCNJ10, Kir4.1, POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 10 
National Institutes of Health

Related topics

Related topics

4 relations
KCNJ10 protein, humanKCNJ12 geneKCNJ14 genepotassium inwardly-rectifying channel, subfamily J, member 10

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Functional implication of KCNJ 10 gene polymorphism in childhood epilepsy
As a commonly occurred brain dysfunction, epilepsy has a sudden onset and is believed to be related with abnormal potassium level… 
2014
2014
Gene Polymorphisms in Childhood Epilepsy KCNJ 10 Contribution of
The purpose of this study was to investigate the possible association between childhood epilepsy and KCNJ10 gene polymorphisms… 
2013
2013
Lijun Wang , Sherin Phosphorylation of KCNJ 10 Protein Distal Convoluted Tubule ( DCT ) by Regulates the Basolateral K Channel in the Src Family Protein Tyrosine Kinase
2010
2010
Altered Renal Tubular Ultrastructure and Electrophysiology Caused by KCNJ10 Mutations in EAST Syndrome
2009
2009
Mutations of KCNJ 10 Together with Mutations of SLC 26 A 4 Cause Digenic Nonsyndromic Hearing Loss Associated with Enlarged Vestibular Aqueduct Syndrome
Mutations in SLC26A4 cause nonsyndromic hearing loss associated with an enlarged vestibular aqueduct (EVA, also known as DFNB4… 
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