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A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Clin Pediatr Endocrinol
Prif Awduron: Nishizaki, Yoshimi, Hiura, Makoto, Sato, Hidetoshi, Ogawa, Yohei, Saitoh, Akihiko, Nagasaki, Keisuke
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The Japanese Society for Pediatric Endocrinology 2016
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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