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

J. Bergoffen, S. S. Scherer, S. Wang, M. Oronzi Scott, L. J. Bone, D. L. Paul, K. Chen, M. W. Lensch, P. F. Chance and K. H. Fischbeck
Science
New Series, Vol. 262, No. 5142 (Dec. 24, 1993), pp. 2039-2042
Stable URL: http://www.jstor.org/stable/2882981
Page Count: 4
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Abstract

X-linked Charcot-Marie-Tooth disease (CMTX) is a form of hereditary neuropathy with demyelination. Recently, this disorder was mapped to chromosome Xq13.1. The gene for the gap junction protein connexin32 is located in the same chromosomal segment, which led to its consideration as a candidate gene for CMTX. With the use of Northern (RNA) blot and immunohistochemistry technique, it was found that connexin32 is normally expressed in myelinated peripheral nerve. Direct sequencing of the connexin32 gene showed seven different mutations in affected persons from eight CMTX families. These findings, a demonstration of inherited defects in a gap junction protein, suggest that connexin32 plays an important role in peripheral nerve.

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