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Book Chapter

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This paper deals with the genetic defect responsible for the X-linked form of Charcot-Marie-Tooth disease.Mutations in the gap junction geneconnexin32(Cx32) cause the X-linked form of Charcot–Marie–Tooth disease, an inherited demyelinating neuropathy.


Published: Fischbeck, Kenneth H., Deschênes, Suzanne M., Bone, Linda Jo, Scherer, Steven. "Connexin32 and X-Linked Charcot-Marie-Tooth Disease." Cold Spring Harbor Symposia on Quantitative Biology LXI Development. Cold Spring Harbor Press, 1996.

At the time of publication Suzanne Deschênes was affiliated with University of Pennsylvania School of Medicine.





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