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Congenital muscular dystrophy with primary partial laminin α2 chain deficiency: Molecular study

Document Type

Article

Author

He, Y.; Vignier, N.; Chevallay, M.; Tomé, F.M.S.; Guicheney, P.; Barois, A.; Estournet-Mathiaud, B.; Jones, K.J.; North, K.N.; Morgan, G.; Hori, H.; Mizuta, T.

Source

In: Neurology. (Neurology, 9 October 2001, 57(7):1319-1322)

Subject

Language

English

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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