valine has been researched along with Rett Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Errijgers, V; Frank Kooy, R; Hayez-Delatte, F; Reyniers, E; Winnepenninckx, B | 1 |
| Afenjar, A; Bahi-Buisson, N; Bienvenu, T; Chelly, J; Girard, B; Nectoux, J; Prieur, F; Rosas-Vargas, H | 1 |
| Bahi-Buisson, N; Bienvenu, T; Chelly, J; Coste, J; De Roux, N; Guellec, I; Nectoux, J; Rosas, H; Tardieu, M | 1 |
3 other study(ies) available for valine and Rett Syndrome
| Article | Year |
|---|---|
Identification of a family with nonspecific mental retardation (MRX79) with the A140V mutation in the MECP2 gene: is there a need for routine screening?
Topics: Alanine; Amino Acid Substitution; Child, Preschool; Chromosomal Proteins, Non-Histone; Chromosomes, Human, X; CpG Islands; DNA-Binding Proteins; Female; Genetic Carrier Screening; Genetic Testing; Haplotypes; Humans; Infant; Intellectual Disability; Male; Methyl-CpG-Binding Protein 2; Mutation; Pedigree; Repressor Proteins; Rett Syndrome; Valine | 2002 |
Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsy.
Topics: Adolescent; Adult; Amino Acid Substitution; Base Sequence; Brain Diseases; Child; Child, Preschool; Epilepsy; Female; Genetic Variation; Glycoproteins; GPI-Linked Proteins; Humans; Leucine; Mutation; Nerve Tissue Proteins; Netrins; Phenotype; Rett Syndrome; Valine | 2007 |
The p.Val66Met polymorphism in the BDNF gene protects against early seizures in Rett syndrome.
Topics: Adolescent; Adult; Brain-Derived Neurotrophic Factor; Child; Cohort Studies; Female; Humans; Methionine; Methyl-CpG-Binding Protein 2; Phenotype; Polymorphism, Genetic; Rett Syndrome; Seizures; Valine | 2008 |