A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1

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Detalles Bibliográficos
Publicado en:Clin Pediatr Endocrinol
Main Authors: Nishizaki, Yoshimi, Hiura, Makoto, Sato, Hidetoshi, Ogawa, Yohei, Saitoh, Akihiko, Nagasaki, Keisuke
Formato: Artigo
Idioma:Inglês
Publicado: The Japanese Society for Pediatric Endocrinology 2016
Assuntos:
Mutation-in-Brief
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5069542/
https://ncbi.nlm.nih.gov/pubmed/27780983
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.25.135
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