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 ChicagoDavid, Stéphanie, et al. "Identification of Partial SLC20A2 Deletions in Primary Brain Calcification Using Whole-exome Sequencing." Eur J Hum Genet 2016.
Citação norma MLADavid, Stéphanie, et al. "Identification of Partial SLC20A2 Deletions in Primary Brain Calcification Using Whole-exome Sequencing." Eur J Hum Genet 2016.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.