Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation)
Dodelson De Kremer, Raquel; Paschini Capra, Ana; Bacman, Sandra; Argaraña, Carlos; Civallero, Gabriel; Kelley, Richard I.; Guelbert, Norberto; Latini, Alexandra; Noher de Halac, Inés; Giner Ayala, Alicia; Johnston, Jennifer; Proujansky, Roy (2001)