Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease
- 1 November 1994
- Vol. 13 (5) , 1253-1260
- https://doi.org/10.1016/0896-6273(94)90063-9
Abstract
No abstract availableThis publication has 48 references indexed in Scilit:
- Charcot-Marie-tooth disease: a new paradigm for the mechanism of inherited diseaseTrends in Genetics, 1994
- Progress in the molecular understanding of hereditary peripheral neuropathies reveals new insights into the biology of the peripheral nervous systemTrends in Neurosciences, 1993
- Gap junctions: New tools, new answers, new questionsNeuron, 1991
- Gap junctions in cultured astrocytes: Single-channel currents and characterization of channel-forming proteinNeuron, 1991
- Protein zero of peripheral nerve myelin: Biosynthesis, membrane insertion, and evidence for homotypic interactionNeuron, 1990
- Sequence and tissue distribution of a second protein of hepatic gap junctions, Cx26, as deduced from its cDNA.The Journal of cell biology, 1989
- Formation of gap junctions by expression of connexins in Xenopus oocyte pairsCell, 1989
- Two homologous protein components of hepatic gap junctionsNature, 1987
- Molecular cloning of cDNA for rat liver gap junction protein.The Journal of cell biology, 1986
- Equilibrium properties of a voltage-dependent junctional conductance.The Journal of general physiology, 1981