Point mutation associated with X-linked dominant Charcot-Marie-Tooth disease impairs the P2 promoter activity of human connexin-32 gene

Cloning and characterization of human and rat liver cDNAs coding for a gap junction protein.

Niranjan M. Kumar, Norton B. Gilula · The Journal of Cell Biology · 1986 · 442 citations · Full text

Life Sciences, Genetics, Molecular Biology +14

Connexin32 is a myelin-related protein in the PNS and CNS

SS Scherer, SM Deschenes, YT Xu et al. · Journal of Neuroscience · 1995 · 410 citations · Full text

Life Sciences, Neurobiology, Neuroscience +14

Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32

P. Anzini, Dirk H.-H. Neuberg, Melitta Schachner et al. · Journal of Neuroscience · 1997 · 312 citations · Full text

Medicine, Neurology, Neuroscience +17

Connexin32-null mice develop demyelinating peripheral neuropathy

Steven S. Scherer, Yitian Xu, Eric Nelles et al. · Glia · 1998 · 302 citations · Full text

Medicine, Neurology, Neuroscience +16

Changes in Permeability Caused by Connexin 32 Mutations Underlie X-Linked Charcot-Marie-Tooth Disease

Seunghoon Oh, Yi Ri, Michael V. L. Bennett et al. · Neuron · 1997 · 248 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9