tryptophan and Cochlear Hearing Loss

tryptophan 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	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Adato, A; Bonné-Tamir, B; Kalinsky, H; Korostishevsky, M; Kwitek-Black, AE; Nystuen, A; Seroussi, E; Sheffield, VC	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 tryptophan and Cochlear Hearing Loss

Article	Year
Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders. American journal of physical anthropology, 1997, Volume: 104, Issue:2 Topics: Arginine; Base Sequence; Chromosomes, Human, Pair 11; Consanguinity; DNA; Female; Genes, Recessive; Genetic Linkage; Genetics, Population; Haplotypes; Hearing Loss, Sensorineural; Humans; Male; Middle East; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Syndrome; Tryptophan; Vestibular Diseases; Vision Disorders	1997
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

Usher syndrome in the Samaritans: strengths and limitations of using inbred isolated populations to identify genes causing recessive disorders.

American journal of physical anthropology, 1997, Volume: 104, Issue:2

Topics: Arginine; Base Sequence; Chromosomes, Human, Pair 11; Consanguinity; DNA; Female; Genes, Recessive; Genetic Linkage; Genetics, Population; Haplotypes; Hearing Loss, Sensorineural; Humans; Male; Middle East; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Single-Stranded Conformational; Syndrome; Tryptophan; Vestibular Diseases; Vision Disorders

1997

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