Order Article Reprints

AlMuhaizea M, Dabbagh O, AlQudairy H, AlHargan A, Alotaibi W, Sami R, AlOtaibi R, Ali MM, AlHindi H, Colak D, et al. Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population. Genes. 2021; 12(11):1783. https://doi.org/10.3390/genes12111783

AlMuhaizea, Mohammad, Omar Dabbagh, Hanan AlQudairy, Aljouhra AlHargan, Wafa Alotaibi, Ruba Sami, Rahaf AlOtaibi, Mariam Mahmoud Ali, Hindi AlHindi, Dilek Colak, and et al. 2021. "Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population" Genes 12, no. 11: 1783. https://doi.org/10.3390/genes12111783

AlMuhaizea, M., Dabbagh, O., AlQudairy, H., AlHargan, A., Alotaibi, W., Sami, R., AlOtaibi, R., Ali, M. M., AlHindi, H., Colak, D., & Kaya, N. (2021). Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population. Genes, 12(11), 1783. https://doi.org/10.3390/genes12111783