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Actininopathy: A new muscular dystrophy caused by ACTN2 dominant mutations

Document Type

Article

Author

Savarese, M.; Vihola, A.; Jonson, P.H.; Sarparanta, J.; Hackman, P.; Udd, B.; Palmio, J.; Poza, J.J.; García-Bragado, F.; Weinberg, J.; Olive, M.; Cobo, A.M.; Urtizberea, J.A.

Source

In: Annals of Neurology. (Annals of Neurology, June 2019, 85(6):899-906)

Subject

Language

English

ISSN

15318249
03645134

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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