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

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Main Author: Josef Finsterer
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Case Reports in Neurological Medicine
Online Access:http://dx.doi.org/10.1155/2020/5846971
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author Josef Finsterer
author_facet Josef Finsterer
author_sort Josef Finsterer
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institution Kabale University
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spelling doaj-art-0139e6b9a9e34797a066ba57d3c2aba52025-02-03T05:51:45ZengWileyCase Reports in Neurological Medicine2090-66682090-66762020-01-01202010.1155/2020/58469715846971Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”Josef Finsterer0Krankenanstalt Rudolfstiftung, Vienna, Austriahttp://dx.doi.org/10.1155/2020/5846971
spellingShingle Josef Finsterer
Comment on “CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions”
Case Reports in Neurological Medicine
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
url http://dx.doi.org/10.1155/2020/5846971
work_keys_str_mv AT joseffinsterer commentoncpeoandmitochondrialmyopathyinapatientwithdguokcompoundheterozygouspathogeneticvariantandmtdnamultipledeletions