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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author Nagasaki, Keisuke
Usui, Takeshi
Asami, Tadashi
Ogawa, Yohei
Kikuchi, Toru
Uchiyama, Makoto
author_facet Nagasaki, Keisuke
Usui, Takeshi
Asami, Tadashi
Ogawa, Yohei
Kikuchi, Toru
Uchiyama, Makoto
author_sort Nagasaki, Keisuke
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spelling pubmed-36876092013-08-07 H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency Nagasaki, Keisuke Usui, Takeshi Asami, Tadashi Ogawa, Yohei Kikuchi, Toru Uchiyama, Makoto Clin Pediatr Endocrinol Mutation-in-Brief The Japanese Society for Pediatric Endocrinology 2009-11-11 2009-10 /pmc/articles/PMC3687609/ /pubmed/23926370 http://dx.doi.org/10.1297/cpe.18.111 Text en 2009©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
Nagasaki, Keisuke
Usui, Takeshi
Asami, Tadashi
Ogawa, Yohei
Kikuchi, Toru
Uchiyama, Makoto
H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
title H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
title_full H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
title_fullStr H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
title_full_unstemmed H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
title_short H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
title_sort h62l mutation of cyp21a2 identified in the non-classical form of 21-hydroxylase deficiency
topic Mutation-in-Brief
url 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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