SMN gene deletion in variant of infantile spinal muscular atrophy

Lancet. 1995 Jul 29;346(8970):316-7. doi: 10.1016/s0140-6736(95)92206-7.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Chromosomes, Human, Pair 5 / genetics*
  • Gene Deletion*
  • Genetic Variation*
  • Heart Defects, Congenital / genetics
  • Homozygote
  • Humans
  • Spinal Muscular Atrophies of Childhood / genetics*