Cita APA

Nemirovsky, S. I., Córdoba, M., Zaiat, J. J., Completa, S. P., Vega, P., González Morón, D., . . . Kauffman, M. A. (2015). Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder. Web

Citación estilo Chicago

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

Cita MLA

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