Chamberlin ME, Ubagai T, Mudd SH, et al. Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene[J]. Am J Hum Genet, 1997, 60(3):540-546.
[4]
Chien YH, Chiang SC, Huang A, et al. Spectrum of hypermethioninemia in neonatal screening[J]. Early Hum Dev, 2005, 81(6):529-533.
[5]
Couce M, Bóveda MD, Castiñeiras DE, et al. Hypermethioninaemia due to methionine adenosyltransferase I/Ⅲ (MAT I/Ⅲ) deficiency:diagnosis in an expanded neonatal screening programme[J]. J Inherit Metab Dis, 2008, 31(Suppl 2):S233-S239.
[6]
Nagao M, Tanaka T, Furujo M. Spectrum of mutations associated with methionine adenosyltransferase I/Ⅲ deficiency among individuals identified during newborn screening in Japan[J]. Mol Genet Metab, 2013, 110(4):460-464.