Advancements in AFG3L2 mutation and neurogenetic disorders: A comprehensive review
December 2024
Neurogenetic disorders are a group of rare and diverse conditions characterized by significant genetic and clinical heterogeneity. Despite their prevalence, the etiology and pathogenic mechanisms of...
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Advances in research on Leber's hereditary optic neuropathy
December 2024
Leber's hereditary optic neuropathy (LHON) is the most prevalent primary mitochondrial DNA (mtDNA) disorder, and the majority of patients carry one of three primary mtDNA point mutations, specifically...
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