An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2

Detalles Bibliográficos
Autores principales: Goda, Takeshi, Komatsu, Hiroshi, Nozu, Kandai, Nakajima, Hisakazu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2020
Materias:
Mutation-in-Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348633/
https://www.ncbi.nlm.nih.gov/pubmed/32694891
http://dx.doi.org/10.1297/cpe.29.127

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7348633/
https://www.ncbi.nlm.nih.gov/pubmed/32694891
http://dx.doi.org/10.1297/cpe.29.127

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