threonine has been researched along with Cochlear Hearing Loss in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dockter, G; Gomes, TS; Gortner, L; Leitner, D; Rohrer, T; Thakker, RV | 1 |
| Borck, G; Martiné, U; Pohlenz, J; Roth, C; Wildhardt, G | 1 |
| Huh, K; Joo, IS; Joo, SY; Ki, CS; Kim, JW | 1 |
| Hatanaka, A; Kimura, A; Kitamura, K; Noguchi, Y; Uzawa, M; Yashima, T; Yasunami, M | 1 |
4 other study(ies) available for threonine and Cochlear Hearing Loss
| 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 |
Mutations in the PDS gene in German families with Pendred's syndrome: V138F is a founder mutation.
Topics: Adolescent; Amino Acid Substitution; Base Sequence; Carrier Proteins; Child; Child, Preschool; Female; Founder Effect; Germany; Haplotypes; Hearing Loss, Sensorineural; Humans; Hypothyroidism; Infant, Newborn; Male; Membrane Transport Proteins; Mutation, Missense; Pedigree; Serine; Sulfate Transporters; Syndrome; Threonine; Turkey | 2003 |
A novel point mutation in PMP22 gene associated with a familial case of Charcot-Marie-Tooth disease type 1A with sensorineural deafness.
Topics: Adult; Arginine; Charcot-Marie-Tooth Disease; DNA Mutational Analysis; Exons; Family Health; Female; Hearing Loss, Sensorineural; Humans; Male; Myelin Proteins; Pedigree; Phenotype; Point Mutation; Threonine | 2004 |
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 |