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Two amino-acid substitutions in the myelin protein zero gene of a case of Charcot–Marie–Tooth disease associated with light-near dissociation

✍ Scribed by H.M.E. Bienfait; F. Baas; A.A.W.M. Gabreëls-Festen; J.H.T.M. Koelman; C.T. Langerhorst; M. de Visser


Book ID
117669491
Publisher
Elsevier Science
Year
2002
Tongue
English
Weight
174 KB
Volume
12
Category
Article
ISSN
0960-8966

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