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Lack of evidence for a pathogenic role of T-lymphocytes in an animal model for Charcot-Marie-Tooth disease 1A

✍ Scribed by Bianca Kohl; Janos Groh; Carsten Wessig; Heinz Wiendl; Antje Kroner; Rudolf Martini


Book ID
113812451
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
982 KB
Volume
38
Category
Article
ISSN
0969-9961

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## Abstract Charcot‐Marie‐Tooth neuropathy type 1A (CMT1A) is the most common inherited neuropathy in humans and is mostly caused by a 1.5‐Mb tandem duplication of chromosome 17 comprising the gene for the peripheral myelin protein 22‐kDa (PMP22). Although there are numerous studies on the function