Cita APA (7a ed.)

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

Cita Chicago Style (17a ed.)

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

Cita MLA (8a ed.)

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