[The importance of genetic diagnosis in an atypical case of spinal muscular atrophy type I]

An Esp Pediatr. 1998 Jun;48(6):644-6.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Exons / genetics
  • Humans
  • Infant, Newborn
  • Male
  • Spinal Muscular Atrophies of Childhood / diagnosis*
  • Spinal Muscular Atrophies of Childhood / genetics*