Associated Papers
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population.
AlMuhaizea M et al.
Genes, 2021
34828389 (PubMed )
Supplement: genes-12-01783-s001.zip › Supplementary_Table_S1.xlsx › Reported_MEGF10_Mutations
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