threonine has been researched along with Deaf Mutism 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 |
|---|---|
| Cranston, T; Gaynor, KU; Gomes, T; Gortner, L; Grigorieva, IV; Nesbit, MA; Thakker, RV | 1 |
| Hatanaka, A; Kimura, A; Kitamura, K; Noguchi, Y; Uzawa, M; Yashima, T; Yasunami, M | 1 |
| Goto, Yi; Nishino, I; Nonaka, I; Oka, Y; Tsukuda, K; Yamasoba, T | 1 |
3 other study(ies) available for threonine and Deaf Mutism
| Article | Year |
|---|---|
A missense GATA3 mutation, Thr272Ile, causes the hypoparathyroidism, deafness, and renal dysplasia syndrome.
Topics: Amino Acid Sequence; Blotting, Western; Deafness; DNA Mutational Analysis; Electrophoretic Mobility Shift Assay; Fluorescent Antibody Technique; GATA3 Transcription Factor; Humans; Hypoparathyroidism; Immunohistochemistry; Infant; Isoleucine; Kidney; Kidney Diseases; Male; Molecular Sequence Data; Mutation, Missense; Syndrome; Threonine | 2009 |
A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.
Topics: Adolescent; Adult; Alanine; Amino Acid Substitution; Auditory Threshold; Child; Codon; Deafness; DNA Mutational Analysis; Exons; Female; Genes, Dominant; Genetic Carrier Screening; Hearing Loss, Sensorineural; Hearing Tests; Humans; Male; Membrane Proteins; Pedigree; Phenotype; Threonine; Wolfram Syndrome | 2005 |
Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.
Topics: Adult; Alanine; Anti-Bacterial Agents; Audiology; Cysteine; Cytochrome b Group; Deafness; DNA, Mitochondrial; Female; Glycine; Hearing; Humans; Male; Middle Aged; Muscle, Skeletal; Mutation; Pedigree; Point Mutation; RNA; RNA, Mitochondrial; RNA, Ribosomal; Streptomycin; Threonine | 2002 |