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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
Päivi Laitinen, Heidi Fodstad, Kirsi Piippo, Heikki Swan, Lauri Toivonen, Matti Viitasalo, Jaakko Kaprio, Kimmo KontulaVolume:
15
Year:
2000
Language:
english
Pages:
2
DOI:
10.1002/1098-1004(200006)15:63.0.co;2-0
File:
PDF, 24 KB
english, 2000