valine and Optic Atrophy, Hereditary, Leber

valine has been researched along with Optic Atrophy, Hereditary, Leber 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	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Akita, Y; Hirata, K; Koga, Y; Povalko, N; Rudenskaia, G; Toyojiro, M; Zakharova, E	1

Other Studies

1 other study(ies) available for valine and Optic Atrophy, Hereditary, Leber

Article	Year
A new sequence variant in mitochondrial DNA associated with high penetrance of Russian Leber hereditary optic neuropathy. Mitochondrion, 2005, Volume: 5, Issue:3 Topics: Amino Acid Substitution; Base Sequence; DNA, Mitochondrial; Female; Genetic Variation; Haplotypes; Humans; Male; Optic Atrophy, Hereditary, Leber; Pedigree; Penetrance; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Russia; Sequence Analysis, DNA; Valine; White People	2005

Article

Year

A new sequence variant in mitochondrial DNA associated with high penetrance of Russian Leber hereditary optic neuropathy.

Mitochondrion, 2005, Volume: 5, Issue:3

Topics: Amino Acid Substitution; Base Sequence; DNA, Mitochondrial; Female; Genetic Variation; Haplotypes; Humans; Male; Optic Atrophy, Hereditary, Leber; Pedigree; Penetrance; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Russia; Sequence Analysis, DNA; Valine; White People

2005