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Paper Details

A loss-of-function nonsynonymous polymorphism in the osmoregulatory TRPV4 gene is associated with human hyponatremia.
Proc Natl Acad Sci U S A
76
2009
Disorders, P19S, Pro, Pro-to-Ser substitution at residue 19, Ser, TRPV4, TRPV4 gene, TRPV4(P19S), TRPV4(P19S) allele, allele, electrolyte disturbances, epoxyeicosatrienoic acid, human, human TRPV4 channel, hyponatremia, minor allele, osmoregulatory TRPV4 gene, sodium, transient receptor potential vanilloid 4
Aged, Alleles, Animals, Cohort Studies, Humans, Hyponatremia, Male, Mice, Mutation, Osteoporosis, Polymorphism, Genetic, Proline, Serine, Sex Factors, TRPV Cation Channels
Author NameAffiliation
Wei TianOregon Health and Science University
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