aica ribonucleotide and Gyrate Atrophy

aica ribonucleotide has been researched along with Gyrate Atrophy 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	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baldoin, MC; Basso, G; Burlina, A; Desbats, MA; Doimo, M; Graziano, C; Lenzini, E; Murphy, E; Salviati, L; Sartori, G; Seri, M; Trevisson, E	1

Other Studies

1 other study(ies) available for aica ribonucleotide and Gyrate Atrophy

Article	Year
Functional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retina. Human mutation, 2013, Volume: 34, Issue:1 Topics: Amino Acid Sequence; Aminoimidazole Carboxamide; Cells, Cultured; DNA Mutational Analysis; Fibroblasts; Genetic Complementation Test; Genetic Predisposition to Disease; Genotype; Gyrate Atrophy; HEK293 Cells; Humans; Immunoblotting; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Ornithine-Oxo-Acid Transaminase; Phenotype; Protein Structure, Tertiary; Ribonucleotides; Saccharomyces cerevisiae; Sequence Homology, Amino Acid	2013

Article

Year

Functional analysis of missense mutations of OAT, causing gyrate atrophy of choroid and retina.

Human mutation, 2013, Volume: 34, Issue:1

Topics: Amino Acid Sequence; Aminoimidazole Carboxamide; Cells, Cultured; DNA Mutational Analysis; Fibroblasts; Genetic Complementation Test; Genetic Predisposition to Disease; Genotype; Gyrate Atrophy; HEK293 Cells; Humans; Immunoblotting; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Ornithine-Oxo-Acid Transaminase; Phenotype; Protein Structure, Tertiary; Ribonucleotides; Saccharomyces cerevisiae; Sequence Homology, Amino Acid

2013