Associated Papers
Expanded spectrum of MEGF10 related myopathies: late-onset myofibrillar myopathy-like phenotype with novel variants.
Zhu B et al.
Neuromuscular Disorders : Nmd, 2026
Congenital myopathy associated with a novel mutation in MEGF10 gene, myofibrillar alteration and progressive course.
Croci C et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology, 2022
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