Linkage of proximal myotonic myopathy to chromosome 3q

Neurology. 1999 Jan 1;52(1):170-1. doi: 10.1212/wnl.52.1.170.

Abstract

We performed genetic linkage analysis in nine German proximal myotonic myopathy (PROMM) families using DNA-markers D3S1541 and D3S1589 from the region of the recently discovered gene locus of myotonic dystrophy type 2 (DM2) on chromosome 3q. Two-point analysis supplied an lod score of 5.9. We conclude that a gene causing PROMM is located on chromosome 3q. PROMM and DM2 may be allelic disorders or may be caused by closely linked genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 3*
  • Genetic Linkage*
  • Genetic Markers
  • Humans
  • Myotonia / genetics*

Substances

  • Genetic Markers