Polymorphism H558R in the Human Cardiac Sodium Channel SCN5A Gene is Associated with Atrial Fibrillation

By Chen L   Zhang W   Fang C   Jiang S   Shu C   Cheng H   Li F   Li H  

The Journal of International Medical Research, Vol. 39, Iss. 5, 2011-09 ,pp. : 1908-1916

Field House Publishing

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Novel Mutation in the KCNJ2 Gene Is Associated with a Malignant Arrhythmic Phenotype of Andersen-Tawil Syndrome

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No Duplicate KRAS Mutation is Identified on the Same Allele in Gastric or Colorectal Cancer Cells with Multiple KRAS Mutations

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Identification of a Novel de novo STK11 Mutation in a Chinese Child with Peutz–Jeghers Syndrome

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Molecular Analysis of a Novel Cathepsin K Gene Mutation in a Chinese Child with Pycnodysostosis

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