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Article

Proof of genetic heterogeneity in the proximal myotonic myopathy syndrome (PROMM) and its relationship to myotonic dystrophy type 2 (DM2).

Neuromuscular disorders : NMD - 1 Oct 2000

Kress W, Mueller-Myhsok B, Ricker K, Schneider C, Koch M C, Toyka K V, Mueller C R, Grimm T

Abstract excerpt

Recently, myotonic dystrophy type 2 has been described as a separate disease entity that is distinctive from classical Steinert's disease since it lacks a CTG repeat expansion on chromosome 19q. A gene locus for myotonic dystrophy type 2 has been mapped to chromosome 3q. Independently, proximal myotonic myopathy has been recognized as yet another form of a multisystem myotonic disorder. Its relationship to...

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PMID: 10996776
DOI: 10.1016/s0960-8966(00)00129-2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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