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

Overview of attention for article published in Human Heredity, September 2008

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Mutations relating to X-linked charcot-marie-tooth disease

Grant US-6001576-A

United States of America

Methods of detecting novel mutations relating to X-linked Charcot-Marie-Tooth disease

Grant US-5691144-A

United States of America

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