SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus
Molecular Genetics & Genomic Medicine2019Vol. 7(9), pp. e892–e892
Citations Over TimeTop 10% of 2019 papers
Sheng Chih Jin, Charuta G. Furey, Xue Zeng, August Allocco, Carol Nelson‐Williams, Weilai Dong, Jason K. Karimy, Kevin Wang, Shaojie Ma, Eric Delpire, Kristopher T. Kahle
Abstract
These findings identify two novel, related genes associated with CH, and implicate genetically encoded impairments in ion transport for the first time in CH pathogenesis.
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