Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1.


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Welzel M., Akin L., Büscher A., Güran T., Hauffa B., Högler W., ...More

European journal of endocrinology, vol.168, pp.707-15, 2013 (SCI-Expanded, Scopus) identifier identifier identifier