A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1

Detalles Bibliográficos
Autores principales: Higuchi, Shinji, Takagi, Masaki, Shimomura, Satoshi, Nishimura, Gen, Hasegawa, Yukihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Pediatric Endocrinology 2016
Materias:
Mutation-in-Brief
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965511/
https://www.ncbi.nlm.nih.gov/pubmed/27507912
http://dx.doi.org/10.1297/cpe.25.107
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author Higuchi, Shinji
Takagi, Masaki
Shimomura, Satoshi
Nishimura, Gen
Hasegawa, Yukihiro
author_facet Higuchi, Shinji
Takagi, Masaki
Shimomura, Satoshi
Nishimura, Gen
Hasegawa, Yukihiro
author_sort Higuchi, Shinji
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spelling pubmed-49655112016-08-09 A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1 Higuchi, Shinji Takagi, Masaki Shimomura, Satoshi Nishimura, Gen Hasegawa, Yukihiro Clin Pediatr Endocrinol Mutation-in-Brief The Japanese Society for Pediatric Endocrinology 2016-07-20 2016-07 /pmc/articles/PMC4965511/ /pubmed/27507912 http://dx.doi.org/10.1297/cpe.25.107 Text en 2016©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
Higuchi, Shinji
Takagi, Masaki
Shimomura, Satoshi
Nishimura, Gen
Hasegawa, Yukihiro
A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1
title A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1
title_full A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1
title_fullStr A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1
title_full_unstemmed A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1
title_short A Japanese familial case of Schmid metaphyseal chondrodysplasia with a novel mutation in COL10A1
title_sort japanese familial case of schmid metaphyseal chondrodysplasia with a novel mutation in col10a1
topic Mutation-in-Brief
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965511/
https://www.ncbi.nlm.nih.gov/pubmed/27507912
http://dx.doi.org/10.1297/cpe.25.107
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