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A novel DNAJB6 mutation causes dominantly inherited distal‐onset myopathy and compromises DNAJB6 function

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Mutations in the DNAJB6 gene have been identified as a rare cause of dominantly inherited limb‐girdle muscular dystrophy or distal‐onset myopathy. Click to show full abstract

Mutations in the DNAJB6 gene have been identified as a rare cause of dominantly inherited limb‐girdle muscular dystrophy or distal‐onset myopathy.

Keywords: distal onset; novel dnajb6; dnajb6 mutation; onset myopathy; dominantly inherited

Journal Title: Clinical Genetics
Year Published: 2017

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