Ramzan, K., Al-Numair, N. S., Al-Ageel, S., Elbaik, L., Sakati, N., Al-Hazzaa, S. A. F., . . . Imtiaz, F. (2020). Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss. Genes (Basel).
Citação norma ChicagoRamzan, Khushnooda, Nouf S. Al-Numair, Sarah Al-Ageel, Lina Elbaik, Nadia Sakati, Selwa A. F. Al-Hazzaa, Mohammed Al-Owain, and Faiqa Imtiaz. "Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss." Genes (Basel) 2020.
Citação norma MLARamzan, Khushnooda, et al. "Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss." Genes (Basel) 2020.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.