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

Detalles Bibliográficos
Autores principales: Nishizaki, Yoshimi, Hiura, Makoto, Sato, Hidetoshi, Ogawa, Yohei, Saitoh, Akihiko, Nagasaki, Keisuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2016
Materias:
Mutation-in-Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069542/
https://www.ncbi.nlm.nih.gov/pubmed/27780983
http://dx.doi.org/10.1297/cpe.25.135

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069542/
https://www.ncbi.nlm.nih.gov/pubmed/27780983
http://dx.doi.org/10.1297/cpe.25.135

Ejemplares similares