Llwytho...
A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Clin Pediatr Endocrinol |
|---|---|
| Prif Awduron: | , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
The Japanese Society for Pediatric Endocrinology
2016
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5069542/ https://ncbi.nlm.nih.gov/pubmed/27780983 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1297/cpe.25.135 |
| Tagiau: |
Ychwanegu Tag
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