arginine has been researched along with Albinism, Oculocutaneous in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (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 |
---|---|
Francke, U; Hsieh, CL; Sekhon, GS; Spritz, RA; Strunk, KM | 1 |
Matsunaga, J; Shibahara, S; Tagami, H; Takeda, A; Tomita, Y | 1 |
2 other study(ies) available for arginine and Albinism, Oculocutaneous
Article | Year |
---|---|
Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinism.
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.
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 |