The X-linked IAP gene does not contribute to the clinical phenotype of spinal muscular atrophy

Clin Genet. 2000 Feb;57(2):154-6. doi: 10.1034/j.1399-0004.2000.570212.x.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alleles
  • Child
  • Child, Preschool
  • Chromosomes, Human, Pair 5
  • DNA, Complementary / metabolism
  • Female
  • Genetic Linkage*
  • Genetic Markers
  • Haplotypes
  • Humans
  • Male
  • Muscular Atrophy, Spinal / genetics*
  • Nerve Tissue Proteins / genetics
  • Neuronal Apoptosis-Inhibitory Protein
  • Pedigree
  • Phenotype
  • Proteins / genetics*
  • X Chromosome*
  • X-Linked Inhibitor of Apoptosis Protein

Substances

  • DNA, Complementary
  • Genetic Markers
  • NAIP protein, human
  • Nerve Tissue Proteins
  • Neuronal Apoptosis-Inhibitory Protein
  • Proteins
  • X-Linked Inhibitor of Apoptosis Protein
  • XIAP protein, human