arginine and Zellweger Syndrome

arginine has been researched along with Zellweger Syndrome in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fujiki, Y; Kondo, N; Kono, T; Nakamura, H; Orii, T; Shimozawa, N; Suzuki, Y; Takada, H; Tomatsu, S; Tsukamoto, T1

Other Studies

1 other study(ies) available for arginine and Zellweger Syndrome

ArticleYear
A novel mutation, R125X in peroxisome assembly factor-1 responsible for Zellweger syndrome.
    Human mutation, 1998, Volume: Suppl 1

    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