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Aldhalaan H, AlBakheet A, AlRuways S, AlMutairi N, AlNakiyah M, AlGhofaili R, Cardona-Londoño KJ, Alahmadi KO, AlQudairy H, AlRasheed MM, et al. A Novel GEMIN4 Variant in a Consanguineous Family Leads to Neurodevelopmental Impairment with Severe Microcephaly, Spastic Quadriplegia, Epilepsy, and Cataracts. Genes. 2022; 13(1):92. https://doi.org/10.3390/genes13010092

Aldhalaan, Hesham, Albandary AlBakheet, Sarah AlRuways, Nouf AlMutairi, Maha AlNakiyah, Reema AlGhofaili, Kelly J. Cardona-Londoño, Khalid Omar Alahmadi, Hanan AlQudairy, Maha M. AlRasheed, and et al. 2022. "A Novel GEMIN4 Variant in a Consanguineous Family Leads to Neurodevelopmental Impairment with Severe Microcephaly, Spastic Quadriplegia, Epilepsy, and Cataracts" Genes 13, no. 1: 92. https://doi.org/10.3390/genes13010092

Aldhalaan, H., AlBakheet, A., AlRuways, S., AlMutairi, N., AlNakiyah, M., AlGhofaili, R., Cardona-Londoño, K. J., Alahmadi, K. O., AlQudairy, H., AlRasheed, M. M., Colak, D., Arold, S. T., & Kaya, N. (2022). A Novel GEMIN4 Variant in a Consanguineous Family Leads to Neurodevelopmental Impairment with Severe Microcephaly, Spastic Quadriplegia, Epilepsy, and Cataracts. Genes, 13(1), 92. https://doi.org/10.3390/genes13010092