Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency.

Ítems similars

• Methionine Adenosyltransferase I/III Deficiency: Novel Mutationsand Clinical Variations
  per: Chamberlin, Margaret E., et al.
  Publicat: (2000)
• Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency.
  per: Ubagai, T, et al.
  Publicat: (1995)
• Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene.
  per: Chamberlin, M E, et al.
  Publicat: (1997)
• Reversible White Matter Lesion in Methionine Adenosyltransferase I/III Deficiency
  per: Tada, Hiroko, et al.
  Publicat: (2004)
• Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations
  per: Nashabat, Marwan, et al.
  Publicat: (2018)