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

類似資料

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