APA

Nemirovsky S. I., Córdoba M., Zaiat J. J., Completa S. P., Vega P. A., González-Morón D., Medina N. M., Fabbro M., Romero S., Brun B., Revale S., Ogara M. F., Pecci A., Marti M., Vazquez M., Turjanski A. & Kauffman M. A. (20160112). Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder. : PloS one.

Chicago

Nemirovsky Sergio I, Córdoba Marta, Zaiat Jonathan J, Completa Sabrina P, Vega Patricia A, González-Morón Dolores, Medina Nancy M, Fabbro Mónica, Romero Soledad, Brun Bianca, Revale Santiago, Ogara María Florencia, Pecci Adali, Marti Marcelo, Vazquez Martin, Turjanski Adrián and Kauffman Marcelo A. 20160112. Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder. : PloS one.

Harvard

Nemirovsky S. I., Córdoba M., Zaiat J. J., Completa S. P., Vega P. A., González-Morón D., Medina N. M., Fabbro M., Romero S., Brun B., Revale S., Ogara M. F., Pecci A., Marti M., Vazquez M., Turjanski A. and Kauffman M. A. (20160112). Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder. : PloS one.

MLA

Nemirovsky Sergio I, Córdoba Marta, Zaiat Jonathan J, Completa Sabrina P, Vega Patricia A, González-Morón Dolores, Medina Nancy M, Fabbro Mónica, Romero Soledad, Brun Bianca, Revale Santiago, Ogara María Florencia, Pecci Adali, Marti Marcelo, Vazquez Martin, Turjanski Adrián and Kauffman Marcelo A. Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder. : PloS one. 20160112.