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UnknownAutosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD.
Not available
S-EPMC3366501 | biostudies-literature
UnknownRecurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism.
Not available
S-EPMC4408447 | biostudies-literature
UnknownMutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities.
Not available
S-EPMC3278668 | biostudies-literature
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