Autosomal Recessive Nonsyndromic Neurosensory Deafness at DFNB1 Not Associated with the Compound-Heterozygous GJB2 (Connexin 26) Genotype M34T/167delT
Open Access
- 1 September 2000
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 67 (3), 745-749
- https://doi.org/10.1086/303045
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Connexin mutations in deafnessNature, 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 sporadic and inherited sensorineural deafnessThe Lancet, 1998
- Connexin mutations and hearing lossNature, 1998
- Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 GeneHuman Molecular Genetics, 1997
- Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated PopulationsHuman Molecular Genetics, 1997
- Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansHuman Molecular Genetics, 1997
- Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessNature, 1997
- CONNEXINS, CONNEXONS, AND INTERCELLULAR COMMUNICATIONAnnual Review of Biochemistry, 1996
- High-yield noninvasive human genomic DNA isolation method for genetic studies in geographically dispersed families and populations.1995