SLC12A ion transporter mutations in sporadic and familial human congenital hydrocephalus.

Jin SC, Furey CG, Zeng X, Allocco A, Nelson-Williams C, Dong W, Karimy JK, Wang K, Ma S, Delpire E, Kahle KT
Mol Genet Genomic Med. 2019 7 (9): e892

PMID: 31393094 · PMCID: PMC6732308 · DOI:10.1002/mgg3.892

MeSH Terms (11)

Animals Cerebral Aqueduct Genetic Diseases, X-Linked Humans Hydrocephalus Male Mutation Neural Cell Adhesion Molecule L1 Symporters Whole Exome Sequencing Xenopus laevis

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