Title : A novel compound heterozygous ROMK mutation presenting as late onset Bartter syndrome associated with nephrocalcinosis and elevated 1,25(OH)(2) vitamin D levels.

Pub. Date : 2011 Aug

PMID : 21431899






1 Functional Relationships(s)
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1 A novel compound heterozygous ROMK mutation presenting as late onset Bartter syndrome associated with nephrocalcinosis and elevated 1,25(OH)(2) vitamin D levels. Vitamin D potassium inwardly rectifying channel subfamily J member 1 Homo sapiens