APA引文

David, S., Ferreira, J., Quenez, O., Rovelet-Lecrux, A., Richard, A., Vérin, M., . . . Nicolas, G. (2016). Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing. Eur J Hum Genet.

Citação norma Chicago

David, Stéphanie, et al. "Identification of Partial SLC20A2 Deletions in Primary Brain Calcification Using Whole-exome Sequencing." Eur J Hum Genet 2016.

MLA引文

David, Stéphanie, et al. "Identification of Partial SLC20A2 Deletions in Primary Brain Calcification Using Whole-exome Sequencing." Eur J Hum Genet 2016.