Ramzan, K.; Al-Numair, N.S.; Al-Ageel, S.; Elbaik, L.; Sakati, N.; Al-Hazzaa, S.A.F.; Al-Owain, M.; Imtiaz, F.
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss. Genes 2020, 11, 1474.
https://doi.org/10.3390/genes11121474
AMA Style
Ramzan K, Al-Numair NS, Al-Ageel S, Elbaik L, Sakati N, Al-Hazzaa SAF, Al-Owain M, Imtiaz F.
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss. Genes. 2020; 11(12):1474.
https://doi.org/10.3390/genes11121474
Chicago/Turabian Style
Ramzan, Khushnooda, Nouf S. Al-Numair, Sarah Al-Ageel, Lina Elbaik, Nadia Sakati, Selwa A. F. Al-Hazzaa, Mohammed Al-Owain, and Faiqa Imtiaz.
2020. "Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss" Genes 11, no. 12: 1474.
https://doi.org/10.3390/genes11121474
APA Style
Ramzan, K., Al-Numair, N. S., Al-Ageel, S., Elbaik, L., Sakati, N., Al-Hazzaa, S. A. F., Al-Owain, M., & Imtiaz, F.
(2020). Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss. Genes, 11(12), 1474.
https://doi.org/10.3390/genes11121474