arginine has been researched along with Zellweger Syndrome in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Fujiki, Y; Kondo, N; Kono, T; Nakamura, H; Orii, T; Shimozawa, N; Suzuki, Y; Takada, H; Tomatsu, S; Tsukamoto, T | 1 |
1 other study(ies) available for arginine and Zellweger Syndrome
Article | Year |
---|---|
A novel mutation, R125X in peroxisome assembly factor-1 responsible for Zellweger syndrome.
Topics: Arginine; Codon, Terminator; DNA; DNA Mutational Analysis; Family Health; Fatal Outcome; Female; Fibroblasts; Humans; Infant; Infant, Newborn; Male; Membrane Proteins; Mutation; Pedigree; Peroxisomal Biogenesis Factor 2; Point Mutation; Zellweger Syndrome | 1998 |