Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.

Published

Journal Article

The two markers most closely linked to the myotonic dystrophy (DM) locus on chromosome 19 are the gene that codes for apolipoprotein CII (APOC2) and the anonymous probe D19S19 (LDR152). Both of these markers show tight linkage to DM, with maximum lod scores of greater than 20 at recombination fractions of less than 0.05. We have identified, in a family in which DM segregates, an affected individual where a meiotic recombination event has occurred in which both of these linked markers have crossed over with the gene defect. This demonstrates that APOC2 and D19S19 are probably on the same side of DM.

Full Text

Cited Authors

  • Johnson, K; Nimmo, E; Jones, P; Weiss, M; Savontaus, ML; Anvret, M; Bartlett, R; Roses, A; Shaw, D; Harper, PS

Published Date

  • December 1988

Published In

Volume / Issue

  • 80 / 4

Start / End Page

  • 379 - 381

PubMed ID

  • 3198115

Pubmed Central ID

  • 3198115

Electronic International Standard Serial Number (EISSN)

  • 1432-1203

International Standard Serial Number (ISSN)

  • 0340-6717

Digital Object Identifier (DOI)

  • 10.1007/bf00273655

Language

  • eng