Connexins, hearing and deafness: clinical aspects of mutations in the connexin 26 gene
- 1 March 2000
- journal article
- review article
- Published by Elsevier in Brain Research Reviews
- Vol. 32 (1) , 159-162
- https://doi.org/10.1016/s0165-0173(99)00075-2
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Mutations in the Connexin 26 Gene (GJB2) among Ashkenazi Jews with Nonsyndromic Recessive DeafnessNew England Journal of Medicine, 1998
- Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratodermaHuman Genetics, 1998
- Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing LossAmerican Journal of Human Genetics, 1998
- Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessNature, 1997
- Genes responsible for human hereditary deafness: symphony of a thousandNature Genetics, 1996
- Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysisBrain Structure and Function, 1995
- Genetic Epidemiology of Hearing ImpairmentAnnals of the New York Academy of Sciences, 1991
- Evoked Mechanical Responses of Isolated Cochlear Outer Hair CellsScience, 1985
- Stimulated acoustic emissions from within the human auditory systemThe Journal of the Acoustical Society of America, 1978
- Audiometric Identification of Normal Hearing Carriers of Genes for DeafnessActa Oto-Laryngologica, 1968