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Myelin sheath protein mutations

Deficiencies of peripheral nerve myelin in common inherited human neuropathies are caused by mutations of genes for sheath proteins 648... [Pg.639]

As noted in the preceding section, Cx32 is a ubiquitous protein that is also found in CNS myelin. Its presence in Schwann cells was discovered when Cx32 mutations were associated with Charcot-Marie-Tooth disease of the CMTX type. CMTX is an X-linked demyelinating neuropathy. The molecule is located in the paranodes. There are subtle anomalies of the myelin sheath and the Ranvier node (Hahn et al.,... [Pg.556]

See other pages where Myelin sheath protein mutations is mentioned: [Pg.1769]    [Pg.69]    [Pg.625]    [Pg.648]    [Pg.649]    [Pg.548]    [Pg.552]    [Pg.286]    [Pg.856]    [Pg.835]    [Pg.81]    [Pg.81]    [Pg.755]   
See also in sourсe #XX -- [ Pg.648 ]



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