Association of the MBL2 gene EXON1 polymorphism and vasoocclusive crisis in patients with sickle cell anemia

Acta Haematol. 2009;121(4):212-5. doi: 10.1159/000220335. Epub 2009 May 26.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Anemia, Sickle Cell / blood
  • Anemia, Sickle Cell / complications*
  • Anemia, Sickle Cell / genetics
  • Child
  • Child, Preschool
  • Exons / genetics
  • Female
  • Gene Frequency
  • Genotype
  • Humans
  • Infant
  • Infant, Newborn
  • Ischemia / etiology*
  • Ischemia / physiopathology
  • Male
  • Mannose-Binding Lectin / blood
  • Mannose-Binding Lectin / deficiency
  • Mannose-Binding Lectin / genetics*
  • Mannose-Binding Lectin / physiology
  • Polymorphism, Single Nucleotide*
  • Recurrence
  • Respiratory Tract Infections / blood
  • Respiratory Tract Infections / complications*

Substances

  • MBL2 protein, human
  • Mannose-Binding Lectin