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First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy

Detalles Bibliográficos
Autores principales: Park, Hyung Jun, Lee, Jung Hwan, Shin, Ha Young, Kim, Seung Min, Lee, Ji Hyun, Choi, Young-Chul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712279/
https://www.ncbi.nlm.nih.gov/pubmed/26320847
http://dx.doi.org/10.3988/jcn.2016.12.1.121
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author Park, Hyung Jun
Lee, Jung Hwan
Shin, Ha Young
Kim, Seung Min
Lee, Ji Hyun
Choi, Young-Chul
author_facet Park, Hyung Jun
Lee, Jung Hwan
Shin, Ha Young
Kim, Seung Min
Lee, Ji Hyun
Choi, Young-Chul
author_sort Park, Hyung Jun
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spelling pubmed-47122792016-01-14 First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy Park, Hyung Jun Lee, Jung Hwan Shin, Ha Young Kim, Seung Min Lee, Ji Hyun Choi, Young-Chul J Clin Neurol Letter to the Editor Korean Neurological Association 2016-01 2015-08-21 /pmc/articles/PMC4712279/ /pubmed/26320847 http://dx.doi.org/10.3988/jcn.2016.12.1.121 Text en Copyright © 2016 Korean Neurological Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to the Editor
Park, Hyung Jun
Lee, Jung Hwan
Shin, Ha Young
Kim, Seung Min
Lee, Ji Hyun
Choi, Young-Chul
First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy
title First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy
title_full First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy
title_fullStr First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy
title_full_unstemmed First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy
title_short First Identification of Compound Heterozygous FKRP Mutations in a Korean Patient with Limb-Girdle Muscular Dystrophy
title_sort first identification of compound heterozygous fkrp mutations in a korean patient with limb-girdle muscular dystrophy
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4712279/
https://www.ncbi.nlm.nih.gov/pubmed/26320847
http://dx.doi.org/10.3988/jcn.2016.12.1.121
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