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
The role of MEGF10 in myoblast fusion and hypertrophic response to overload of skeletal muscle.
Richardson L et al.
Journal of Muscle Research and Cell Motility, 2025
Phenotypic Variability of MEGF10 Variants Causing Congenital Myopathy: Report of Two Unrelated Patients from a Highly Consanguineous Population.
AlMuhaizea M et al.
Genes, 2021
Adult-onset respiratory insufficiency, scoliosis, and distal joint hyperlaxity in patients with multiminicore disease due to novel Megf10 mutations.
Liewluck T et al.
Muscle & Nerve, 2016
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