Novel Mutations in the Connexin 26 Gene (GJB2) That Cause Autosomal Recessive (DFNB1) Hearing Loss
- 1 April 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (4) , 792-799
- https://doi.org/10.1086/301807
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessNature, 1997
- Connections with Connexins: the Molecular Basis of Direct Intercellular SignalingEuropean Journal of Biochemistry, 1996
- The connexin family of intercellular channel forming proteinsKidney International, 1995
- Coordination of vertebrate cellular assemblies by gap junctionsSeminars in Developmental Biology, 1995
- New functions for gap junctionsCurrent Opinion in Cell Biology, 1995
- A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene intervalHuman Molecular Genetics, 1994
- Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth diseaseNeuron, 1994
- Opposite voltage gating polarities of two closely related onnexinsNature, 1994
- Gap junctions in the brain: where, what type, how many and why?Trends in Neurosciences, 1993
- Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines.The Journal of cell biology, 1992