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scnn1a protein human
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A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mu…
A Novel SCNN1A Variation in a Patient with Autosomal-recessive Pseudohypoaldosteronism Type 1
Clinical and genetic characteristics of the patients with hypertension and hypokalemia carrying a no…
Association between low-sodium salt intervention and long-term blood pressure changes is modified by…
Extracellular vesicles regulate purinergic signaling and epithelial sodium channel expression in ren…
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