proline has been researched along with Decreased Muscle Tone in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Anderson, G; Benatti, M; Brown, R; Chong, K; Clayton, PT; Footitt, E; Gissen, P; Hemingway, C; Holden, S; James, C; Little, D; Mills, PB; Ocaka, L; Parker, A; Rahman, S; Reid, ES; Williams, H | 1 |
| Arné-Bes, MC; Delisle, MB; Figarella-Branger, D; Heitz, F; Levade, T; Pellissier, JF; Richard, P; Uro-Coste, E | 1 |
2 other study(ies) available for proline and Decreased Muscle Tone
| Article | Year |
|---|---|
Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay.
Topics: Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Developmental Disabilities; Female; Fibroblasts; Glutamic Acid; Humans; Infant; Infant, Newborn; Male; Mitochondria; Mitochondria, Liver; Mitochondrial Membrane Transport Proteins; Muscle Hypotonia; Mutation; Proline; Seizures | 2017 |
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.
Topics: Amino Acid Substitution; Cardiac Myosins; Cardiomyopathies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heart; Humans; Leucine; Middle Aged; Muscle Hypotonia; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Myosin Heavy Chains; Phenotype; Proline; Young Adult | 2009 |