Cita APA (7a ed.)

Dodelson De Kremer, R., Paschini Capra, A., Bacman, S., Argaraña, C., Civallero, G., Kelley, R. I., . . . Proujansky, R. (2001). Barth's syndrome-like disorder: A new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).

Cita Chicago Style (17a ed.)

Dodelson De Kremer, Raquel, et al. Barth's Syndrome-like Disorder: A New Phenotype with a Maternally Inherited A3243G Substitution of Mitochondrial DNA (MELAS Mutation). 2001.

Cita MLA (8a ed.)

Dodelson De Kremer, Raquel, et al. Barth's Syndrome-like Disorder: A New Phenotype with a Maternally Inherited A3243G Substitution of Mitochondrial DNA (MELAS Mutation). 2001.