Associated Papers
Rhabdomyolysis associated with OBSCN mutations: case report and mechanistic review.
Liu Q et al.
Neuromuscular Disorders : Nmd, 2025
Identification of Compound Heterozygous Variants in OBSCN Gene Associated With Rhabdomyolysis: A Case Report.
Sun X et al.
Molecular Genetics & Genomic Medicine, 2025
Age and Sex Differences in the Genetics of Cardiomyopathy.
Akinrinade O et al.
Journal of Cardiovascular Translational Research, 2023
37477868 (PubMed )
Supplement: 12265_2023_10411_MOESM1_ESM.xlsx › Table_S2_All_variants
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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