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Myotonic dystrophy type 2

25 Feb 2003

Abstract excerpt

BACKGROUND: Myotonic dystrophy types 1 (DM1) and 2 (DM2/proximal myotonic myopathy PROMM) are dominantly inherited disorders with unusual multisystemic clinical features. The authors have characterized the clinical and molecular features of DM2/PROMM, which is caused by a CCTG repeat expansion in intron 1 of the zinc finger protein 9 (ZNF9) gene. METHODS: Three-hundred and seventy-nine individuals from 133...

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Identifiers

PMID: 12601109
DOI: 10.1212/01.wnl.0000054481.84978.f9

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Source receipt: pubmed, retrieved 7 Sept 2026.

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