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A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia

✍ Scribed by M. Luigetti; A. Modoni; R. Renna; G. Silvestri; E. Ricci; N. Montano; G. Tasca; M. Papacci; M. Monforte; A. Conte; M.G. Pomponi; M. Sabatelli


Book ID
116369769
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
345 KB
Volume
112
Category
Article
ISSN
0303-8467

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