Browsing by Author "Saada, A."
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- ItemFatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation(2016) Spiegel, R.; Saada, A.; Flannery, P.; Burte, F.; Soiferman, D.; Khayat, M.; Eisner Sagüés, Verónica Raquel; Vladovski, E.; Taylor, R.; Bindoff, L.; Shaag, A.; Mandel, H.; Schuler, O.; Shalev, S.; Elpeleg, O.; Yu, P.