A polymorphic synonymous mutation in human ornithine-δ-aminotransferase (N378N)

Ítems similars

• An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.
  per: Mitchell, G A, et al.
  Publicat: (1988)
• Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation.
  per: Mitchell, G A, et al.
  Publicat: (1991)
• Ornithine δ-aminotransferase: An enzyme implicated in salt tolerance in higher plants
  per: Stránská, Jana, et al.
  Publicat: (2008)
• Two continuous coupled assays for ornithine-δ-aminotransferase
  per: Juncosa, Jose I, et al.
  Publicat: (2013)
• Ornithine-δ-aminotransferase is essential for Arginine Catabolism but not for Proline Biosynthesis
  per: Funck, Dietmar, et al.
  Publicat: (2008)