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STUB1 mutations in autosomal recessive ataxias - evidence for mutation-specific clinical heterogeneity

Document Type

Article

Author

Heimdal, K.; Sanchez-Guixé, M.; Aukrust, I.; Bollerslev, J.; Bruland, O.; Jablonski, G.E.; Erichsen, A.K.; Gude, E.; Koht, J.A.; Erdal, S.; Fiskerstrand, T.; Haukanes, B.I.; Boman, H.; Bjørkhaug, L.; Tallaksen, C.M.; Knappskog, P.M.; Johansson, S.

Source

In: Orphanet journal of rare diseases. (Orphanet journal of rare diseases, 2014, 9:146)

Subject

Language

English

ISSN

17501172

Online Access

Full Text (Gale Academic Onefile) Full Text (ProQuest Central) Open Access (EBSCO) Open Access (BioMed Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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