Cargando…

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy

Detalles Bibliográficos
Autores principales: Finsterer, Josef, Zarrouk-Mahjoub, Sinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658547/
https://www.ncbi.nlm.nih.gov/pubmed/28883250
http://dx.doi.org/10.2169/internalmedicine.8820-17
_version_ 1783274024915173376
author Finsterer, Josef
Zarrouk-Mahjoub, Sinda
author_facet Finsterer, Josef
Zarrouk-Mahjoub, Sinda
author_sort Finsterer, Josef
collection PubMed
description
format Online
Article
Text
id pubmed-5658547
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher The Japanese Society of Internal Medicine
record_format MEDLINE/PubMed
spelling pubmed-56585472017-10-27 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy Finsterer, Josef Zarrouk-Mahjoub, Sinda Intern Med Letters to the Editor The Japanese Society of Internal Medicine 2017-09-06 2017-10-01 /pmc/articles/PMC5658547/ /pubmed/28883250 http://dx.doi.org/10.2169/internalmedicine.8820-17 Text en Copyright © 2017 by The Japanese Society of Internal Medicine https://creativecommons.org/licenses/by-nc-nd/4.0/ The Internal Medicine is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Letters to the Editor
Finsterer, Josef
Zarrouk-Mahjoub, Sinda
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
title Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
title_full Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
title_fullStr Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
title_full_unstemmed Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
title_short Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
title_sort mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (melas) due to a m.10158t>c nd3 mutation with a normal muscle biopsy
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658547/
https://www.ncbi.nlm.nih.gov/pubmed/28883250
http://dx.doi.org/10.2169/internalmedicine.8820-17
work_keys_str_mv AT finstererjosef mitochondrialmyopathyencephalopathylacticacidosisandstrokelikeepisodesmelasduetoam10158tcnd3mutationwithanormalmusclebiopsy
AT zarroukmahjoubsinda mitochondrialmyopathyencephalopathylacticacidosisandstrokelikeepisodesmelasduetoam10158tcnd3mutationwithanormalmusclebiopsy