Page last updated: 2024-08-17

methionine and Glycine Encephalopathy

methionine has been researched along with Glycine Encephalopathy in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ben-Neriah, Z; Boneh, A; Kanno, J; Korman, SH; Kure, S; Lerer, I; Matsubara, Y; Sato, K	1

Other Studies

1 other study(ies) available for methionine and Glycine Encephalopathy

Article	Year
A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem. Journal of human genetics, 2005, Volume: 50, Issue:5 Topics: Amino Acid Oxidoreductases; Amino Acid Substitution; Arabs; Codon, Initiator; Female; Glycine; Glycine Dehydrogenase (Decarboxylating); Humans; Hyperglycinemia, Nonketotic; Israel; Male; Methionine; Pedigree; Point Mutation; RNA, Messenger; Threonine	2005

Article

Year

A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem.

Journal of human genetics, 2005, Volume: 50, Issue:5

Topics: Amino Acid Oxidoreductases; Amino Acid Substitution; Arabs; Codon, Initiator; Female; Glycine; Glycine Dehydrogenase (Decarboxylating); Humans; Hyperglycinemia, Nonketotic; Israel; Male; Methionine; Pedigree; Point Mutation; RNA, Messenger; Threonine

2005