A start codon CMT1X mutation associated with transient encephalomyelitis causes complete loss of Cx32

Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease

JoAnn Bergoffen, S. S. Scherer, S. Wang et al. · Science · 1993 · 1.1K citations

Medicine, Genetics, Molecular Genetics +16

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

Connexins Are Critical for Normal Myelination in the CNS

Daniela M. Menichella, Daniel A. Goodenough, Erich E. Sirkowski et al. · Journal of Neuroscience · 2003 · 301 citations · Full text

Medicine, Neurobiology, Neuroscience +17

Mutations in the Gene Encoding Gap Junction Protein α12 (Connexin 46.6) Cause Pelizaeus-Merzbacher–Like Disease

Birgit Uhlenberg, Markus Schuelke, Franz Rüschendorf et al. · The American Journal of Human Genetics · 2004 · 272 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Connexin 47 (Cx47)-Deficient Mice with Enhanced Green Fluorescent Protein Reporter Gene Reveal Predominant Oligodendrocytic Expression of Cx47 and Display Vacuolized Myelin in the CNS

Benjamin Odermatt, Kerstin Wellershaus, Anke Wallraff et al. · Journal of Neuroscience · 2003 · 259 citations · Full text

Medicine, Neurobiology, Neuroscience +17