@article {1354344,
	title = {Optic atrophy and a Leigh-like syndrome due to mutations in the c12orf65 gene: report of a novel mutation and review of the literature},
	journal = {J Neuroophthalmol},
	volume = {34},
	number = {1},
	year = {2014},
	month = {2014 Mar},
	pages = {39-43},
	abstract = {Combined oxidative phosphorylation deficiency type 7 (COXPD7) is a rare disorder of mitochondrial metabolism that results in optic atrophy and Leigh syndrome-like disease. We describe 2 siblings with compound heterozygous mutations in the recently identified C12orf65 gene who presented with optic atrophy and mild developmental delays and subsequently developed bilateral, symmetric lesions in the brainstem reminiscent of Leigh syndrome. Repeat neuroimaging demonstrated reversibility of the findings in 1 sibling and persistent metabolic stroke in the other. This article highlights the phenotypic manifestations from a novel mutation in the C12orf65 gene and reviews the clinical presentation of the 5 other individuals reported to date who carry mutations in this gene.},
	keywords = {Child, Child, Preschool, DNA, DNA Mutational Analysis, Female, Follow-Up Studies, Humans, Leigh Disease, Magnetic Resonance Imaging, Male, Mitochondrial Proteins, Mutation, Optic Atrophy, Peptide Termination Factors, Phenotype, Siblings},
	issn = {1536-5166},
	doi = {10.1097/WNO.0000000000000076},
	author = {Heidary, Gena and Calderwood, Laurel and Cox, Gerald F and Robson, Caroline D and Teot, Lisa A and Mullon, Jennifer and Anselm, Irina}
}
