Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation)

por 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
Publicado 2001