threonine has been researched along with Nephrosis 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 | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Dockter, G; Gomes, TS; Gortner, L; Leitner, D; Rohrer, T; Thakker, RV | 1 |
1 other study(ies) available for threonine and Nephrosis
Article | Year |
---|---|
HDR syndrome: a follow-up genotype-phenotype analysis of a de novo missense Thr272Ile mutation in exon 4 of GATA3.
Topics: Child; Child, Preschool; Combined Modality Therapy; Developmental Disabilities; DNA Mutational Analysis; Exons; Follow-Up Studies; GATA3 Transcription Factor; Genetic Carrier Screening; Genotype; Hearing Loss, Sensorineural; Humans; Hypoparathyroidism; Infant; Isoleucine; Male; Mutation, Missense; Nephrosis; Phenotype; Threonine | 2012 |