Commentary: New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (M.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2
Frontiers in Immunology - Switzerland
doi 10.3389/fimmu.2019.01333
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June 21, 2019
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Frontiers Media SA