Associated Papers
A mild and transient form of autosomal recessive pseudohypoaldosteronism type 1 caused by a novel mutation in the SCNN1A gene.
Efthymiadou A et al.
American Journal of Physiology. Endocrinology and Metabolism, 2023
A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population.
Alzahrani AS et al.
Journal of the Endocrine Society, 2021
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