leucine and Cochlear Hearing Loss

leucine has been researched along with Cochlear Hearing Loss in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Berman, Z; Leshinsky-Silver, E; Lev, D; Vinkler, C; Yannov-Sharav, M	1
Ayadi, H; Charfedine, I; Drira, M; Elgaied-Boulila, A; Ghorbel, AM; Grati, M; Hardelin, JP; Hmani, M; Masmoudi, S	1

Other Studies

2 other study(ies) available for leucine and Cochlear Hearing Loss

Article	Year
A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness. Hearing research, 2005, Volume: 202, Issue:1-2 Topics: Alleles; Base Sequence; Child; Connexin 26; Connexins; Conserved Sequence; Cytosine; Female; Genes, Recessive; Hearing Loss, Sensorineural; Homozygote; Humans; Leucine; Mutation, Missense; Point Mutation; Polymorphism, Restriction Fragment Length; Proline; Thymine	2005
Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation. American journal of medical genetics, 2000, Jan-03, Volume: 90, Issue:1 Topics: Adolescent; Adult; Amino Acid Substitution; Carrier Proteins; Child; Child, Preschool; Female; Goiter; Hearing Loss, Sensorineural; Humans; Leucine; Male; Membrane Transport Proteins; Middle Aged; Mutation, Missense; Pedigree; Phenotype; Sulfate Transporters; Tryptophan	2000

Article

Year

A novel missense mutation in the Connexin 26 gene associated with autosomal recessive sensorineural deafness.

Hearing research, 2005, Volume: 202, Issue:1-2

Topics: Alleles; Base Sequence; Child; Connexin 26; Connexins; Conserved Sequence; Cytosine; Female; Genes, Recessive; Hearing Loss, Sensorineural; Homozygote; Humans; Leucine; Mutation, Missense; Point Mutation; Polymorphism, Restriction Fragment Length; Proline; Thymine

2005

Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation.

American journal of medical genetics, 2000, Jan-03, Volume: 90, Issue:1

Topics: Adolescent; Adult; Amino Acid Substitution; Carrier Proteins; Child; Child, Preschool; Female; Goiter; Hearing Loss, Sensorineural; Humans; Leucine; Male; Membrane Transport Proteins; Middle Aged; Mutation, Missense; Pedigree; Phenotype; Sulfate Transporters; Tryptophan

2000