The MELAS phenotype may not only be determined by heteroplasmy of causative mtDNA variants

in European Journal of Endocrinology
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  • 1 Klinik Landstrasse, Messerli Institute, Vienna, Austria

Correspondence should be addressed to J Finsterer; Email: fifigs1@yahoo.de
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     European Society of Endocrinology

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  • 1

    Chae HW, Na JH, Kim HS & Lee YM Mitochondrial diabetes and mitochondrial DNA mutation load in MELAS syndrome. European Journal of Endocrinology 2020 183 505512. (https://doi.org/10.1530/EJE-20-0189)

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    Reed EM, Swanson AA, Roden AC & Lin PT Sudden unexpected death in MELAS syndrome due to diabetic ketoacidosis. American Journal of Forensic Medicine and Pathology 2020 41 331332. (https://doi.org/10.1097/PAF.0000000000000563)

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    Chu CC, Huang CC, Fang W, Chu NS, Pang CY & Wei YH Peripheral neuropathy in mitochondrial encephalomyopathies. European Neurology 1997 37 11011 5. (https://doi.org/10.1159/000117420)

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