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- W1970749810 abstract "CHARCOT-MARIE-TOOTH DISEASE (also known as hereditary motor and sensory neuropathy) is the most commonly inherited peripheral polyneuropathy, with an incidence of 1 in 2,600. 1 Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth’s disease. Clin Genet. 1974; 6: 98-118 Crossref PubMed Scopus (718) Google Scholar Charcot-Marie-Tooth disease (CMTD) occurs as a consequence of several modes of genetic transmission (including autosomal dominant, autosomal recessive, and X-linked forms), and causes variable degrees of peripheral nerve demyelination and Schwann cell dysfunction by producing myelin or gap junction protein abnormalities. 2 Bergoffen J. Scherer S.S. Wang S. et al. Connexin mutations in X-linked Charcot-Marie-Tooth disease. Science. 1993; 262: 2039-2042 Crossref PubMed Scopus (974) Google Scholar , 3 Su Y. Brooks D.G. Li L. et al. Myelin protein zero gene mutated in Charcot-Marie-Tooth type 1B patients. Proc Natl Acad Sci USA. 1993; 90: 10856-10860 Crossref PubMed Scopus (75) Google Scholar" @default.
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- W1970749810 date "2007-08-01" @default.
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- W1970749810 title "Perioperative Implications of Charcot-Marie-Tooth Disease During Coronary Artery Bypass Graft Surgery" @default.
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