Linkage studies in facioscapulohumeral muscular dystrophy

Muscle Nerve. 1988 Aug;11(8):833-5. doi: 10.1002/mus.880110806.

Abstract

Possible linkage between the locus for autosomal dominant facioscapulo-humeral muscular dystrophy and the locus for the constant region of the heavy chains of the IgG immunoglobulins (Gm) was tested in 1 kindred (23 affected and 18 unaffected sibs) using the polymorphic DNA probe D14S1, which is known to be closely linked with Gm. No linkage between the loci for the disease and the probe was found, and the lod scores suggested that the locus for facioscapulohumeral muscular dystrophy is not situated on the distal part of the long arm of chromosome 14.

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 14*
  • DNA Probes
  • Female
  • Genes, Dominant*
  • Genetic Linkage*
  • Humans
  • Immunoglobulin Constant Regions / genetics
  • Immunoglobulin Heavy Chains / genetics
  • Male
  • Muscular Dystrophies / genetics*
  • Pedigree

Substances

  • DNA Probes
  • Immunoglobulin Constant Regions
  • Immunoglobulin Heavy Chains