Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes

J Med Genet. 2003 Dec;40(12):e132. doi: 10.1136/jmg.40.12.e132.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Arrhythmias, Cardiac / diagnosis
  • Arrhythmias, Cardiac / genetics
  • Cardiomyopathy, Dilated / diagnosis
  • Cardiomyopathy, Dilated / genetics
  • Child
  • DNA Mutational Analysis
  • Heart Diseases / genetics*
  • Humans
  • Lamin Type A / genetics*
  • Lamins / genetics*
  • Membrane Proteins / genetics
  • Middle Aged
  • Muscular Dystrophies / diagnosis
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophy, Emery-Dreifuss / diagnosis
  • Muscular Dystrophy, Emery-Dreifuss / genetics
  • Mutation*
  • Nuclear Proteins
  • Phenotype
  • Thymopoietins / genetics

Substances

  • Lamin Type A
  • Lamins
  • Membrane Proteins
  • Nuclear Proteins
  • Thymopoietins
  • emerin

Associated data

  • OMIM/115200
  • OMIM/159001

Grants and funding