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

    Phenotypic Variability of <i>MEGF10</i> Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population by Mohammad AlMuhaizea, Omar Dabbagh, Hanan AlQudairy, Aljouhra AlHargan, Wafa Alotaibi, Ruba Sami, Rahaf AlOtaibi, Mariam Mahmoud Ali, Hindi AlHindi, Dilek Colak, Namik Kaya

    Published 2021-11-01
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