Novel MT-ND Gene Variants Causing Adult-Onset Mitochondrial Disease and Isolated Complex I Deficiency

Mitochondrial complex I deficiency is associated with a diverse range of clinical phenotypes and can arise due to either mitochondrial DNA (mtDNA) or nuclear gene defects. We investigated two adult patients who exhibited non-syndromic neurological features and evidence of isolated mitochondrial comp...

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Detalles Bibliográficos
Autores principales: Ng, Yi Shiau, Thompson, Kyle, Loher, Daniela, Hopton, Sila, Falkous, Gavin, Hardy, Steven A., Schaefer, Andrew M., Shaunak, Sandip, Roberts, Mark E., Lilleker, James B., Taylor, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052259/
https://www.ncbi.nlm.nih.gov/pubmed/32158465
http://dx.doi.org/10.3389/fgene.2020.00024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7052259/
https://www.ncbi.nlm.nih.gov/pubmed/32158465
http://dx.doi.org/10.3389/fgene.2020.00024

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