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P43 Genetic modifying factors for the common form of CMT1A due to the chromosome 17 duplication and other causes of CMT1 in non-CMT1A patients

✍ Scribed by A. Pandraud; S.M. Murphy; M. Laurá; M.M. Reilly; H. Houlden


Book ID
117670361
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
38 KB
Volume
21
Category
Article
ISSN
0960-8966

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