Cita APA (7a ed.)

Nemirovsky, S. I., Ogara, M. F., Pecci, A., Martí, M. A., Vazquez, M. P., & Turjanski, A. G. (2015). Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder.

Cita Chicago Style (17a ed.)

Nemirovsky, Sergio I., Maria Florencia Ogara, Adali Pecci, Marcelo Adrián Martí, Martín Pablo Vazquez, y Adrián Gustavo Turjanski. Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder. 2015.

Cita MLA (8a ed.)

Nemirovsky, Sergio I., et al. Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder. 2015.