Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects

✍ Scribed by Päivi Laitinen; Heidi Fodstad; Kirsi Piippo; Heikki Swan; Lauri Toivonen; Matti Viitasalo; Jaakko Kaprio; Kimmo Kontula

• Publisher: John Wiley and Sons
• Year: 2000
• Tongue: English
• Weight: 24 KB
• Volume: 15
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/1098-1004(200006)15:6<580::aid-humu16>3.0.co;2-0