Title : Coexistence of autosomal dominant polycystic kidney disease type 1 and hereditary renal hypouricemia type 2: A model of early-onset and fast cyst progression.

Pub. Date : 2020 Jun

PMID : 32166738






1 Functional Relationships(s)
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1 This is the first case of coexistence of PKD1 and SLC2A9 mutations treated with tolvaptan. Tolvaptan polycystin 1, transient receptor potential channel interacting Homo sapiens