H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency

Detalles Bibliográficos
Autores principales: Nagasaki, Keisuke, Usui, Takeshi, Asami, Tadashi, Ogawa, Yohei, Kikuchi, Toru, Uchiyama, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2009
Materias:
Mutation-in-Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687609/
https://www.ncbi.nlm.nih.gov/pubmed/23926370
http://dx.doi.org/10.1297/cpe.18.111

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687609/
https://www.ncbi.nlm.nih.gov/pubmed/23926370
http://dx.doi.org/10.1297/cpe.18.111

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