Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency.

Eitemau Tebyg

• Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency.
  gan: Chamberlin, M E, et al.
  Cyhoeddwyd: (1996)
• Methionine Adenosyltransferase I/III Deficiency: Novel Mutationsand Clinical Variations
  gan: Chamberlin, Margaret E., et al.
  Cyhoeddwyd: (2000)
• Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene.
  gan: Chamberlin, M E, et al.
  Cyhoeddwyd: (1997)
• Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency.
  gan: Gahl, W A, et al.
  Cyhoeddwyd: (1988)
• Hepatic methionine adenosyltransferase deficiency in a 31-year-old man.
  gan: Gahl, W A, et al.
  Cyhoeddwyd: (1987)