Search Results - Pfeiffer, Ryan
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Overlapping LQT1 and LQT2 phenotype in a patient with long QT syndrome associated with loss-of-function variations in KCNQ1 and KCNH2 by Cordeiro, Jonathan M. (Author) , Perez, Guillermo J. (Author) , Schmitt, Nicole (Author) , Pfeiffer, Ryan (Author) , Nesterenko, Vladislav V. (Author) , Burashnikov, Elena (Author) , Veltmann, Christian (Author) , Borggrefe, Martin (Author) , Wolpert, Christian (Author) , Schimpf, Rainer (Author) , Antzelevitch, Charles (Author) ,
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Adult
Amino Acid Sequence
Animals
Base Sequence
CHO Cells
Cells, Cultured
Cricetinae
Cricetulus
ERG1 Potassium Channel
Electrocardiography
Ether-A-Go-Go Potassium Channels
Female
Genetic Variation
Humans
KCNQ1 Potassium Channel
Long QT Syndrome
Molecular Sequence Data
Mutation
Phenotype
Polymorphism, Genetic