%0 Journal Article
%T Comment on ¡°CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions¡±
%A Finsterer
%A Josef
%J -
%D 2020
%R https://doi.org/10.1155/2020/5846971
%X With interest, we read the article by Montano et al. about a 42-year-old Italian female with ptosis, ophthalmoparesis, dysphagia, exercise intolerance, and myalgias [1]. The phenotype was attributed to the compound heterozygous mutations c.462T>A and c.707£¿+£¿2T>G in the DGUOK gene secondarily causing multiple mtDNA deletions [1]. We have the following comments and concerns
%U https://www.hindawi.com/journals/crinm/2020/5846971/