Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population

por AlMuhaizea, Mohammad, Dabbagh, Omar, AlQudairy, Hanan, AlHargan, Aljouhra, Alotaibi, Wafa, Sami, Ruba, AlOtaibi, Rahaf, Ali, Mariam Mahmoud, AlHindi, Hindi, Colak, Dilek, Kaya, Namik
Publicado 2021