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
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author Goda, Takeshi
Komatsu, Hiroshi
Nozu, Kandai
Nakajima, Hisakazu
author_facet Goda, Takeshi
Komatsu, Hiroshi
Nozu, Kandai
Nakajima, Hisakazu
author_sort Goda, Takeshi
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spelling pubmed-73486332020-07-20 An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2 Goda, Takeshi Komatsu, Hiroshi Nozu, Kandai Nakajima, Hisakazu Clin Pediatr Endocrinol Mutation-in-Brief The Japanese Society for Pediatric Endocrinology 2020-07-11 2020 /pmc/articles/PMC7348633/ /pubmed/32694891 http://dx.doi.org/10.1297/cpe.29.127 Text en 2020©The Japanese Society for Pediatric Endocrinology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: http://creativecommons.org/licenses/by-nc-nd/4.0/）.
spellingShingle Mutation-in-Brief
Goda, Takeshi
Komatsu, Hiroshi
Nozu, Kandai
Nakajima, Hisakazu
An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
title An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
title_full An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
title_fullStr An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
title_full_unstemmed An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
title_short An infantile case of pseudohypoaldosteronism type 1 (PHA1) caused by a novel mutation of NR3C2
title_sort infantile case of pseudohypoaldosteronism type 1 (pha1) caused by a novel mutation of nr3c2
topic Mutation-in-Brief
url 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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