5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia.

Ítems similars

• Enzymatic defect in "X-linked" sideroblastic anemia: molecular evidence for erythroid delta-aminolevulinate synthase deficiency.
  per: Cotter, P D, et al.
  Publicat: (1992)
• Sequence of human 5-aminolevulinate synthase cDNA.
  per: Bawden, M J, et al.
  Publicat: (1987)
• Late-onset X-linked sideroblastic anemia. Missense mutations in the erythroid delta-aminolevulinate synthase (ALAS2) gene in two pyridoxine-responsive patients initially diagnosed with acquired refractory anemia and ringed sideroblasts.
  per: Cotter, P D, et al.
  Publicat: (1995)
• X-linked sideroblastic anemia and ataxia: linkage to phosphoglycerate kinase at Xq13.
  per: Raskind, W H, et al.
  Publicat: (1991)
• Erythroid 5-aminolevulinate synthase is located on the X chromosome.
  per: Cox, T C, et al.
  Publicat: (1990)