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Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy.

Document Type

journal article

Author

Nelis, E; Erdem, S; Van Den Bergh, P Y K; Belpaire-Dethiou, M-C; Ceuterick, C; Van Gerwen, V; Cuesta, A; Pedrola, L; Palau, F; Gabreëls-Festen, A A W M; Verellen, C; Tan, E; Demirci, M; Van Broeckhoven, C; De Jonghe, P; Topaloglu, H; Timmerman, V

Source

Neurology; 2002 Dec 24, Vol. 59 Issue 12, p1865-1872, 8p

Subject

Language

ISSN

00283878

Online Access

Full Text (LWW Journals - Ovid) Full Text (LWW total - Ovid) Full Text (LWW Premier Journals) Web of Science JCR 저널정보 Scopus Find it@PNU

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