Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by M. L. Marquardt
Mutation of an A-Kinase-Anchoring Protein Causes Long-Qt Syndrome
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Related publications
R231C Mutation in KCNQ1 Causes Long QT Syndrome Type 1 and Familial Atrial Fibrillation
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Novel Deletion Mutation in the Cardiac Sodium Channel Inactivation Gate Causes Long QT Syndrome
International Journal of Cardiology
Cardiovascular Medicine
Cardiology
Novel Mutation in the Per-Arnt-Sim Domain of KCNH2 Causes a Malignant Form of Long-Qt Syndrome
Circulation
Cardiovascular Medicine
Physiology
Cardiology
An InterdomainKCNH2Mutation Produces an Intermediate Long QT Syndrome
Human Mutation
Genetics
A-Kinase Anchoring Protein-Calcineurin Signaling in Long-Term Depression of GABAergic Synapses
Journal of Neuroscience
Neuroscience
Congenital Long QT Syndrome
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Familial Long QT Syndrome
Mutation Detection in Long QT Syndrome: A Comprehensive Set of Primers and PCR Conditions
Journal of Medical Genetics
Genetics
Parmacogenomics of Long QT Syndrome
Japanese Journal of Clinical Pharmacology and Therapeutics
Pharmacology