phenylalanine has been researched along with Deaf Mutism in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| de Zwart-Storm, EA; Martin, PE; Steijlen, PM; van Geel, M; van Neer, PA; van Steensel, MA | 1 |
| Baumann, H; Berlin, A; Lubs, H; Peters, WH; Rose, HJ | 1 |
1 trial(s) available for phenylalanine and Deaf Mutism
| Article | Year |
|---|---|
[Histidine tolerance in low skin histidase activity].
Topics: Adolescent; Adult; Ammonia-Lyases; Child; Chromatography, Thin Layer; Clinical Trials as Topic; Deafness; Female; Histidine; Histidine Ammonia-Lyase; Humans; Imidazoles; Male; Phenylalanine; Skin | 1975 |
1 other study(ies) available for phenylalanine and Deaf Mutism
| Article | Year |
|---|---|
A novel missense mutation in the second extracellular domain of GJB2, p.Ser183Phe, causes a syndrome of focal palmoplantar keratoderma with deafness.
Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Child, Preschool; Connexin 26; Connexins; Conserved Sequence; Deafness; DNA Mutational Analysis; Female; Hearing Loss, Sensorineural; HeLa Cells; Humans; Keratoderma, Palmoplantar; Male; Molecular Sequence Data; Mutation, Missense; Pedigree; Phenotype; Phenylalanine; Protein Structure, Tertiary; Recombinant Fusion Proteins; Serine; Syndrome | 2008 |