Analysis of Mitochondrial DNA Sequences in Childhood Encephalomyopathies Reveals New Disease-Associated Variants

BACKGROUND: Mitochondrial encephalomyopathies are a heterogeneous group of clinical disorders generally caused due to mutations in either mitochondrial DNA (mtDNA) or nuclear genes encoding oxidative phosphorylation (OXPHOS). We analyzed the mtDNA sequences from a group of 23 pediatric patients with...

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Detalles Bibliográficos
Autores principales: Wani, Aijaz A., Ahanger, Sajad H., Bapat, Sharmila A., Rangrez, Ashraf Y., Hingankar, Nitin, Suresh, C. G., Barnabas, Shama, Patole, Milind S., Shouche, Yogesh S.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976591/
https://www.ncbi.nlm.nih.gov/pubmed/17895983
http://dx.doi.org/10.1371/journal.pone.0000942

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1976591/
https://www.ncbi.nlm.nih.gov/pubmed/17895983
http://dx.doi.org/10.1371/journal.pone.0000942

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