Kurul, S. H., Matalonga, L., Paramonov, I., Laurie, S., Beltran, S., Lochmüller, H., & Horvath, R. (2022). High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases.
Citação norma ChicagoKurul, Semra Hiz, Leslie Matalonga, Ida Paramonov, Steven Laurie, Sergi Beltran, Hanns Lochmüller, e Rita Horvath. High Diagnostic Rate of Trio Exome Sequencing in Consanguineous Families With Neurogenetic Diseases. 2022.
Citação norma MLAKurul, Semra Hiz, et al. High Diagnostic Rate of Trio Exome Sequencing in Consanguineous Families With Neurogenetic Diseases. 2022.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.