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Myopathy with MTCYB mutation mimicking Multiple Acyl-CoA Dehydrogenase Deficiency

Document Type

Short Communication

Author

Kaphan, E.; Bou Ali, H.; Gastaldi, M.; Acquaviva, C.; Vianey-Saban, C.; Rouzier, C.; Fragaki, K.; Bannwarth, S.; Paquis-Flucklinger, V.; Romero, N.; Behin, A.; Lombès, A.; Jardel, C.; Rigal, O.; Laforêt, P.

Source

In Revue Neurologique December 2018 174(10):731-735

Subject

Language

ISSN

0035-3787

Online Access

Full Text (ScienceDirect 종량제) Web of Science JCR 저널정보 Scopus Find it@PNU

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