Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy

Detalles Bibliográficos
Autores principales: Xia, Yu, Feng, Yijie, Xu, Lu, Chen, Xiaoyang, Gao, Feng, Mao, Shanshan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204803/
https://www.ncbi.nlm.nih.gov/pubmed/34140971
http://dx.doi.org/10.3389/fgene.2021.684042
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author Xia, Yu
Feng, Yijie
Xu, Lu
Chen, Xiaoyang
Gao, Feng
Mao, Shanshan
author_facet Xia, Yu
Feng, Yijie
Xu, Lu
Chen, Xiaoyang
Gao, Feng
Mao, Shanshan
author_sort Xia, Yu
collection PubMed
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spelling pubmed-82048032021-06-16 Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy Xia, Yu Feng, Yijie Xu, Lu Chen, Xiaoyang Gao, Feng Mao, Shanshan Front Genet Genetics Frontiers Media S.A. 2021-06-01 /pmc/articles/PMC8204803/ /pubmed/34140971 http://dx.doi.org/10.3389/fgene.2021.684042 Text en Copyright © 2021 Xia, Feng, Xu, Chen, Gao and Mao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Xia, Yu
Feng, Yijie
Xu, Lu
Chen, Xiaoyang
Gao, Feng
Mao, Shanshan
Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy
title Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy
title_full Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy
title_fullStr Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy
title_full_unstemmed Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy
title_short Corrigendum: Case Report: Whole-Exome Sequencing With MLPA Revealed Variants in Two Genes in a Patient With Combined Manifestations of Spinal Muscular Atrophy and Duchenne Muscular Dystrophy
title_sort corrigendum: case report: whole-exome sequencing with mlpa revealed variants in two genes in a patient with combined manifestations of spinal muscular atrophy and duchenne muscular dystrophy
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8204803/
https://www.ncbi.nlm.nih.gov/pubmed/34140971
http://dx.doi.org/10.3389/fgene.2021.684042
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