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Description
In contrast to FSHD2 individuals, BAMS patients show no signs of muscular dystrophy while SMCHD1 mutations in FSHD2 are not associated with craniofacial defects, which are characteristic for BAMS

Wang W, Zhang J, Wang Y, Xu Y, Zhang S

The differences among the isoforms have been explained in detail by Butterfield and Mattson (2020)

It can reduce peroxidized polyunsaturated fatty acids through the catalysis of GPX4, thereby inhibiting ferroptosis

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doi: 10.1016/j.phrs.2015.07.021
