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Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype

Neurodegenerative DiseasesMendelian DisorderMitochondrial FunctionNovel Homozygous VariantMitochondrial DynamicGeneticsGenetic DisorderMitochondrial MedicineMolecular GeneticsNeurologyDisease Gene IdentificationRecurrent Stroke-like EpisodesMedicine