Leigh Syndrome: A Tale of Two Genomes
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DOI: 10.3389/fphys.2021.693734
Abstract: Leigh syndrome is a rare, complex, and incurable early onset (typically infant or early childhood) mitochondrial disorder with both phenotypic and genetic heterogeneity. The heterogeneous nature of this disorder, based in part on the complexity… read more here.
Keywords: leigh syndrome; etiology; tale two; syndrome tale ... See more keywords