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
Consequences of MEGF10 deficiency on myoblast function and Notch1 interactions.
Saha M et al.
Human Molecular Genetics, 2017
Japanese multiple epidermal growth factor 10 (MEGF10) myopathy with novel mutations: A phenotype-genotype correlation.
Takayama K et al.
Neuromuscular Disorders : Nmd, 2016
Cysteine mutations cause defective tyrosine phosphorylation in MEGF10 myopathy.
Mitsuhashi S et al.
Febs Letters, 2013
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