arginine and Albinism, Oculocutaneous

arginine has been researched along with Albinism, Oculocutaneous in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Francke, U; Hsieh, CL; Sekhon, GS; Spritz, RA; Strunk, KM1
Matsunaga, J; Shibahara, S; Tagami, H; Takeda, A; Tomita, Y1

Other Studies

2 other study(ies) available for arginine and Albinism, Oculocutaneous

ArticleYear
Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism.
    American journal of human genetics, 1991, Volume: 48, Issue:2

    Topics: Adult; Albinism, Oculocutaneous; Alleles; Arginine; Black People; Blotting, Southern; Codon; Cysteine; DNA; Exons; Homozygote; Humans; Male; Monophenol Monooxygenase; Mutation; Nucleic Acid Hybridization; Polymerase Chain Reaction; Polymorphism, Genetic

1991
Molecular basis of tyrosinase-negative oculocutaneous albinism. A single base mutation in the tyrosinase gene causing arginine to glutamine substitution at position 59.
    The Journal of biological chemistry, 1990, Oct-15, Volume: 265, Issue:29

    Topics: Albinism, Oculocutaneous; Arginine; Base Sequence; Exons; Female; Genes; Genotype; Glutamine; Humans; Introns; Male; Molecular Sequence Data; Monophenol Monooxygenase; Mutation; Pedigree; Promoter Regions, Genetic; Restriction Mapping

1990