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NOS1AP Is a Genetic Modifier of Congenital Long-QT Syndrome

✍ Scribed by Crotti, Lia; Insolia, Roberto; Monti, Maria Cristina; Pedrazzini, Matteo; Taravelli, Erika; Peljto, Anna; Goosen, Althea; Brink, Paul A.; Greenberg, David A.; Schwartz, Peter J.


Book ID
122614932
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
94 KB
Volume
6
Category
Article
ISSN
1547-5271

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