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A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Japanese Society for Pediatric Endocrinology
2016
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| Materias: | |
| 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 |
| _version_ | 1782460955287879680 |
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| author | Nishizaki, Yoshimi Hiura, Makoto Sato, Hidetoshi Ogawa, Yohei Saitoh, Akihiko Nagasaki, Keisuke |
| author_facet | Nishizaki, Yoshimi Hiura, Makoto Sato, Hidetoshi Ogawa, Yohei Saitoh, Akihiko Nagasaki, Keisuke |
| author_sort | Nishizaki, Yoshimi |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-5069542 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2016 |
| publisher | The Japanese Society for Pediatric Endocrinology |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-50695422016-10-25 A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1 Nishizaki, Yoshimi Hiura, Makoto Sato, Hidetoshi Ogawa, Yohei Saitoh, Akihiko Nagasaki, Keisuke Clin Pediatr Endocrinol Mutation-in-Brief The Japanese Society for Pediatric Endocrinology 2016-10-18 2016-10 /pmc/articles/PMC5069542/ /pubmed/27780983 http://dx.doi.org/10.1297/cpe.25.135 Text en 2016©The Japanese Society for Pediatric Endocrinology http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. |
| spellingShingle | Mutation-in-Brief Nishizaki, Yoshimi Hiura, Makoto Sato, Hidetoshi Ogawa, Yohei Saitoh, Akihiko Nagasaki, Keisuke A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1 |
| title | A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1 |
| title_full | A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1 |
| title_fullStr | A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1 |
| title_full_unstemmed | A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1 |
| title_short | A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1 |
| title_sort | novel mutation in the human mineralocorticoid receptor gene in a japanese family with autosomal-dominant pseudohypoaldosteronism type 1 |
| topic | Mutation-in-Brief |
| url | 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 |
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