A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1

Detalles Bibliográficos
Autores principales: Tsunogai, Toshiki, Miyata, Ichiro, Kotake, Saori, Matsuura, Ryuki, Takagi, Ken, Nanba, Hiroyuki, Takahata, Noriko, Tajima, Toshihiro, Wada, Yasuyuki
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/PMC4965512/
https://www.ncbi.nlm.nih.gov/pubmed/27507913
http://dx.doi.org/10.1297/cpe.25.111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965512/
https://www.ncbi.nlm.nih.gov/pubmed/27507913
http://dx.doi.org/10.1297/cpe.25.111

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