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pseudohypoaldosteronism type ii
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OMIM - Aldosterone disorder
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A young child with pseudohypoaldosteronism type II by a mutation of Cullin 3.
CUL3 gene analysis enables early intervention for pediatric pseudohypoaldosteronism type II in infan…
Phenotypes of pseudohypoaldosteronism type II caused by the WNK4 D561A missense mutation are depende…
Mechanisms for hypercalciuria in pseudohypoaldosteronism type II-causing WNK4 knock-in mice.
Identification of a novel WNK4 mutation in Chinese patients with pseudohypoaldosteronism type II.
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Phase II Study of the Pathophysiology and Treatment With Enalapril and Polystyrene Sulfonate for Pse…
Baby Detect : Genomic Newborn Screening
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