connexin 32

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Consortium Fine Localization of X-Linked Charcot-Marie-Tooth Disease (CMTX1): Additional Support that Connexin32 Is the Defect in CMTX1

Margaret A. Pericak-Vance,David F. Barker,Joann Bergoffen,Phillip Chance,Susan Cochrane,Niklas Dahl,...

1995 human heredity DOI: 10.1159/000154272 206 views

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linkage neuropathy x-linked charcot-marie-tooth disease x chromosome