valine and Hearing Loss

valine has been researched along with Hearing Loss 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
Başaran, S; Başerer, N; Brunner, HG; Caylan, R; Cremers, CW; Erdol, H; Hafiz, G; Heister, AJ; Hennies, HC; Kalay, E; Karaguzel, A; Kayserili, H; Kremer, H; Krieger, E; Nürnberg, P; Ulubil-Emiroglu, M; Uyguner, O; Uzumcu, A; Wollnik, B	1

Other Studies

1 other study(ies) available for valine and Hearing Loss

Article	Year
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation. American journal of medical genetics. Part A, 2007, Oct-15, Volume: 143A, Issue:20 Topics: Base Sequence; DNA Mutational Analysis; Haplotypes; Hearing Loss; Homozygote; Humans; Hydrophobic and Hydrophilic Interactions; Models, Molecular; Molecular Sequence Data; Mutation; Myosins; Pedigree; Protein Structure, Tertiary; Turkey; Valine	2007

Article

Year

MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.

American journal of medical genetics. Part A, 2007, Oct-15, Volume: 143A, Issue:20

Topics: Base Sequence; DNA Mutational Analysis; Haplotypes; Hearing Loss; Homozygote; Humans; Hydrophobic and Hydrophilic Interactions; Models, Molecular; Molecular Sequence Data; Mutation; Myosins; Pedigree; Protein Structure, Tertiary; Turkey; Valine

2007