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Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System.

Document Type

Article

Author

Bezzina, Connie R.; Rook, Martin B.; Groenewegen, W. Antoinette; Herfst, Lucas J.; van der Wal, Allard C.; Lam, Jan; Jongsma, Habo J.; Wilde, Arthur A.M.; Mannens, Marcel M.A.M.

Source

Circulation Research; 2/7/2003, Vol. 92 Issue 2, p159-168, 10p

Subject

Language

ISSN

00097330

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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