Bonnet, C., Riahi, Z., Chantot-Bastaraud, S., Smagghe, L., Letexier, M., Marcaillou, C., . . . Petit, C. (2016). An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients. Eur J Hum Genet.
Citação norma ChicagoBonnet, Crystel, et al. "An Innovative Strategy for the Molecular Diagnosis of Usher Syndrome Identifies Causal Biallelic Mutations in 93% of European Patients." Eur J Hum Genet 2016.
Citação norma MLABonnet, Crystel, et al. "An Innovative Strategy for the Molecular Diagnosis of Usher Syndrome Identifies Causal Biallelic Mutations in 93% of European Patients." Eur J Hum Genet 2016.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.