valine has been researched along with Prader-Willi Syndrome 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 | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (100.00) | 2.80 |
Authors | Studies |
---|---|
Atwal, PS; Bersten, DC; Blackburn, PR; Caulfield, TR; Cooiman, M; Gerassimou, AG; Harris, KG; Klee, EW; Kleinendorst, L; Ross, OA; Sullivan, AE; van Gerpen, JA; van Haelst, MM; Whitelaw, ML; Wierenga, KJ | 1 |
1 other study(ies) available for valine and Prader-Willi Syndrome
Article | Year |
---|---|
Functional Analysis of the SIM1 Variant p.G715V in 2 Patients With Obesity.
Topics: Adult; Amino Acid Substitution; Basic Helix-Loop-Helix Transcription Factors; Genetic Association Studies; Glutamic Acid; Humans; Male; Middle Aged; Mutation, Missense; Obesity; Prader-Willi Syndrome; Repressor Proteins; Valine | 2020 |