Associated Papers
Identification of Compound Heterozygous Variants in OBSCN Gene Associated With Rhabdomyolysis: A Case Report.
Sun X et al.
Molecular Genetics & Genomic Medicine, 2025
Novel OBSCN variants associated with a risk to exercise-intolerance and rhabdomyolysis.
Zemorshidi F et al.
Neuromuscular Disorders : Nmd, 2024
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis.
Cabrera-Serrano M et al.
Brain : a Journal of Neurology, 2022
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