Spiegel, R., Saada, A., Flannery, P. J., Burté, F., Soiferman, D., Khayat, M., . . . Yu-Wai-Man, P. (2016). Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation. J Med Genet.
Style de citation ChicagoSpiegel, Ronen, et al. "Fatal Infantile Mitochondrial Encephalomyopathy, Hypertrophic Cardiomyopathy and Optic Atrophy Associated With a Homozygous OPA1 Mutation." J Med Genet 2016.
Style de citation MLASpiegel, Ronen, et al. "Fatal Infantile Mitochondrial Encephalomyopathy, Hypertrophic Cardiomyopathy and Optic Atrophy Associated With a Homozygous OPA1 Mutation." J Med Genet 2016.
Attention : ces citations peuvent ne pas être correctes à 100%.