cystathionine and Electron Transport Chain Deficiencies, Mitochondrial

cystathionine has been researched along with Electron Transport Chain Deficiencies, Mitochondrial 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
Atkison, P; Feigenbaum, A; Hegele, RA; Kronick, J; Rupar, A; Tadiboyina, VT; Wang, J	1

Other Studies

1 other study(ies) available for cystathionine and Electron Transport Chain Deficiencies, Mitochondrial

Article	Year
Novel mutation in DGUOK in hepatocerebral mitochondrial DNA depletion syndrome associated with cystathioninuria. American journal of medical genetics. Part A, 2005, Jun-15, Volume: 135, Issue:3 Topics: Amino Acid Sequence; Base Sequence; Cystathionine; Cystathionine gamma-Lyase; DNA; DNA Mutational Analysis; DNA, Mitochondrial; Hepatolenticular Degeneration; Humans; Infant; Mitochondrial Diseases; Mutation; Phosphotransferases (Alcohol Group Acceptor); Siblings; Syndrome	2005

Article

Year

Novel mutation in DGUOK in hepatocerebral mitochondrial DNA depletion syndrome associated with cystathioninuria.

American journal of medical genetics. Part A, 2005, Jun-15, Volume: 135, Issue:3

Topics: Amino Acid Sequence; Base Sequence; Cystathionine; Cystathionine gamma-Lyase; DNA; DNA Mutational Analysis; DNA, Mitochondrial; Hepatolenticular Degeneration; Humans; Infant; Mitochondrial Diseases; Mutation; Phosphotransferases (Alcohol Group Acceptor); Siblings; Syndrome

2005