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Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”

Detalles Bibliográficos
Autor principal: Finsterer, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154966/
https://www.ncbi.nlm.nih.gov/pubmed/32308999
http://dx.doi.org/10.1155/2020/5846971
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spelling pubmed-71549662020-04-17 Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions” Finsterer, Josef Case Rep Neurol Med Letter to the Editor Hindawi 2020-03-07 /pmc/articles/PMC7154966/ /pubmed/32308999 http://dx.doi.org/10.1155/2020/5846971 Text en Copyright © 2020 Josef Finsterer. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letter to the Editor
Finsterer, Josef
Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
title Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
title_full Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
title_fullStr Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
title_full_unstemmed Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
title_short Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
title_sort comment on “cpeo and mitochondrial myopathy in a patient with dguok compound heterozygous pathogenetic variant and mtdna multiple deletions”
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7154966/
https://www.ncbi.nlm.nih.gov/pubmed/32308999
http://dx.doi.org/10.1155/2020/5846971
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