AlMuhaizea, M.; Dabbagh, O.; AlQudairy, H.; AlHargan, A.; Alotaibi, W.; Sami, R.; AlOtaibi, R.; Ali, M.M.; 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, 1783.
https://doi.org/10.3390/genes12111783
AMA Style
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
Chicago/Turabian Style
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
APA Style
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