isoleucine and Retinitis Pigmentosa

isoleucine has been researched along with Retinitis Pigmentosa in 2 studies

Research

Studies (2)

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

Authors	Studies
Briard, ML; Chatelin, S; Dufier, JL; Gerber, S; Ghazi, I; Kaplan, J; Michel-Awad, A; Munnich, A; Perrault, I; Plessis, G; Rozet, JM; Segues, B; Souied, E	1
Akeo, K; Kudoh, J; Mashima, Y; Oguchi, Y; Saga, M; Shimizu, N	1

Other Studies

2 other study(ies) available for isoleucine and Retinitis Pigmentosa

Article	Year
Severe manifestations in carrier females in X linked retinitis pigmentosa. Journal of medical genetics, 1997, Volume: 34, Issue:10 Topics: Adolescent; Adult; Arginine; Carrier Proteins; Child; Child, Preschool; Chromosome Mapping; Eye Proteins; Female; Genetic Linkage; Genetic Markers; Heterozygote; Humans; Isoleucine; Male; Middle Aged; Pedigree; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Retinitis Pigmentosa; X Chromosome	1997
A novel homozygous Ile535Asn mutation in the rod cGMP phosphodiesterase beta-subunit gene in two brothers of a Japanese family with autosomal recessive retinitis pigmentosa. Current eye research, 1998, Volume: 17, Issue:3 Topics: 3',5'-Cyclic-GMP Phosphodiesterases; Adult; Asparagine; Codon; Cyclic Nucleotide Phosphodiesterases, Type 6; Fundus Oculi; Humans; Isoleucine; Japan; Male; Middle Aged; Pedigree; Phosphoric Diester Hydrolases; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Retinal Rod Photoreceptor Cells; Retinitis Pigmentosa; Visual Fields	1998

Article

Year

Severe manifestations in carrier females in X linked retinitis pigmentosa.

Journal of medical genetics, 1997, Volume: 34, Issue:10

Topics: Adolescent; Adult; Arginine; Carrier Proteins; Child; Child, Preschool; Chromosome Mapping; Eye Proteins; Female; Genetic Linkage; Genetic Markers; Heterozygote; Humans; Isoleucine; Male; Middle Aged; Pedigree; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Retinitis Pigmentosa; X Chromosome

1997

A novel homozygous Ile535Asn mutation in the rod cGMP phosphodiesterase beta-subunit gene in two brothers of a Japanese family with autosomal recessive retinitis pigmentosa.

Current eye research, 1998, Volume: 17, Issue:3

Topics: 3',5'-Cyclic-GMP Phosphodiesterases; Adult; Asparagine; Codon; Cyclic Nucleotide Phosphodiesterases, Type 6; Fundus Oculi; Humans; Isoleucine; Japan; Male; Middle Aged; Pedigree; Phosphoric Diester Hydrolases; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Retinal Rod Photoreceptor Cells; Retinitis Pigmentosa; Visual Fields

1998