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Article

Analysis of mitochondrial DNA sequences in childhood encephalomyopathies reveals new disease-associated variants.

PloS one - 26 Sept 2007

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

Abstract excerpt

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 clinical and morphological features of mitochondrial encephalopathies and tried to establish a relationship of...

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Identifiers

PMID: 17895983
DOI: 10.1371/journal.pone.0000942
PMCID: PMC1976591

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