threonine and Wolfram Syndrome

threonine has been researched along with Wolfram Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Hatanaka, A; Kimura, A; Kitamura, K; Noguchi, Y; Uzawa, M; Yashima, T; Yasunami, M	1

Other Studies

1 other study(ies) available for threonine and Wolfram Syndrome

Article	Year
A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss. Acta oto-laryngologica, 2005, Volume: 125, Issue:11 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

Article

Year

A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss.

Acta oto-laryngologica, 2005, Volume: 125, Issue:11

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