Homozygosity for autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) does not result in a more severe phenotype

J Med Genet. 2004 Feb;41(2):e17. doi: 10.1136/jmg.2003.010637.
No abstract available

Publication types

  • Case Reports
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Genes, Dominant / genetics*
  • Homozygote*
  • Humans
  • Male
  • Muscular Dystrophy, Facioscapulohumeral / diagnosis*
  • Muscular Dystrophy, Facioscapulohumeral / genetics*
  • Pedigree
  • Phenotype