isoleucine has been researched along with Spastic Paraplegia, Hereditary in 1 studies
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 | Studies |
---|---|
Blair, M; Fenichel, GM; Haines, JL; Hedera, P | 1 |
1 other study(ies) available for isoleucine and Spastic Paraplegia, Hereditary
Article | Year |
---|---|
Novel mutation in the SPG3A gene in an African American family with an early onset of hereditary spastic paraplegia.
Topics: Adolescent; Adult; Black or African American; Child; Child, Preschool; Chromosomes, Human, Pair 14; DNA Mutational Analysis; Family Health; Female; Genotype; GTP Phosphohydrolases; GTP-Binding Proteins; Humans; Isoleucine; Male; Membrane Proteins; Middle Aged; Mutation; Pedigree; Spastic Paraplegia, Hereditary; Threonine | 2004 |