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Leigh Syndrome: A Tale of Two Genomes

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 of mitochondrial genetics, and the significant interact...

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Detalles Bibliográficos
Autores principales:	Bakare, Ajibola B., Lesnefsky, Edward J., Iyer, Shilpa
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Physiology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8385445/ https://www.ncbi.nlm.nih.gov/pubmed/34456746 http://dx.doi.org/10.3389/fphys.2021.693734

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