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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

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