Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome

Detalles Bibliográficos
Autores principales: Fu, Jun, Ma, Ming-Ming, Pang, Mi, Yang, Liang, Li, Gang, Song, Jia, Zhang, Jie-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Correspondence
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595846/
https://www.ncbi.nlm.nih.gov/pubmed/30897601
http://dx.doi.org/10.1097/CM9.0000000000000151
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author Fu, Jun
Ma, Ming-Ming
Pang, Mi
Yang, Liang
Li, Gang
Song, Jia
Zhang, Jie-Wen
author_facet Fu, Jun
Ma, Ming-Ming
Pang, Mi
Yang, Liang
Li, Gang
Song, Jia
Zhang, Jie-Wen
author_sort Fu, Jun
collection PubMed
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spelling pubmed-65958462019-07-02 Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome Fu, Jun Ma, Ming-Ming Pang, Mi Yang, Liang Li, Gang Song, Jia Zhang, Jie-Wen Chin Med J (Engl) Correspondence Wolters Kluwer Health 2019-04-05 2019-04-05 /pmc/articles/PMC6595846/ /pubmed/30897601 http://dx.doi.org/10.1097/CM9.0000000000000151 Text en Copyright © 2019 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Correspondence
Fu, Jun
Ma, Ming-Ming
Pang, Mi
Yang, Liang
Li, Gang
Song, Jia
Zhang, Jie-Wen
Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome
title Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome
title_full Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome
title_fullStr Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome
title_full_unstemmed Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome
title_short Broadening the phenotype of m.5703G>A mutation in mitochondrial tRNA(Asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome
title_sort broadening the phenotype of m.5703g>a mutation in mitochondrial trna(asn) gene from mitochondrial myopathy to myoclonic epilepsy with ragged red fibers syndrome
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595846/
https://www.ncbi.nlm.nih.gov/pubmed/30897601
http://dx.doi.org/10.1097/CM9.0000000000000151
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