Cite
MLA Citation
Ronen Spiegel et al.. “Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation.” Journal of medical genetics, vol. 53, no. 2, 2016, pp. 127–131. http://access.bl.uk/ark:/81055/vdc_100135163567.0x000033