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researchers discovered a gene that causes the most common form of muscular dystrophy in adults
On Apr. 15. 2021, a team of researchers led by the University of Minnesota Medical School announced they had found mutations in a novel gene that may help identify patients with a specific form of muscular dystrophy.
The team found a novel gene associated with muscular dystrophy and described a group of 13 families from around the world affected by muscular dystrophy who harbor disease-causing mutations in a gene named JAG2.
The group found a distinct pattern of abnormalities on muscle MRI that may help identify other patients with this specific form of muscular dystrophy in the future.
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Source: University of Minnesota
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