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KCNH2-K897T is a genetic modifier of latent congenital long-QT syndrome

Document Type

Journal

Author

Crotti, L; Lundquist, AL; Insolia, R; Pedrazzini, M; Ferrandi, C; De Ferrari, GM; Vicentini, A; Yang, P; Roden, DM; George, AL; Schwartz, PJ

Source

CIRCULATION; AUG 30 2005, 112 9, p1251-p1258, 8p.

Subject

Language

English

ISSN

00097322

Online Access

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

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