Cita APA

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.

Citación estilo Chicago

Kurul, Semra Hiz, Leslie Matalonga, Ida Paramonov, Steven Laurie, Sergi Beltran, Hanns Lochmüller, y Rita Horvath. High Diagnostic Rate of Trio Exome Sequencing in Consanguineous Families With Neurogenetic Diseases. 2022.

Cita MLA

Kurul, Semra Hiz, et al. High Diagnostic Rate of Trio Exome Sequencing in Consanguineous Families With Neurogenetic Diseases. 2022.