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Publications by Simon Mégy
A Novel Alpha Cardiac Actin (ACTC1) Mutation Mapping to a Domain in Close Contact With Myosin Heavy Chain Leads to a Variety of Congenital Heart Defects, Arrhythmia and Possibly Midline Defects
PLoS ONE
Multidisciplinary
Related publications
Comprehensive Approach to Congenital Heart Defects
Journal of Cardiovascular Disease Research
Cardiovascular Medicine
Cardiology
Recruitment of a Myosin Heavy Chain Kinase to Actin-Rich Protrusions in Dictyostelium
Current Biology
Genetics
Molecular Biology
Biochemistry
Biological Sciences
Neuroscience
Agricultural
Identification of a Mutation in the Beta Cardiac Myosin Heavy Chain Gene in a Family With Hypertrophic Cardiomyopathy.
Heart
Cardiovascular Medicine
Cardiology
A Gain-Of-Function Mutation in the M-Domain of Cardiac Myosin-Binding Protein-C Increases Binding to Actin
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Ankyrin Repeat Domain 1: A Novel Gene for Cardiac Septal Defects
Journal of Gene Medicine
Molecular Medicine
Drug Discovery
Genetics
Molecular Biology
Vulnerability of the Developing Heart to Oxygen Deprivation as a Cause of Congenital Heart Defects
Journal of the American Heart Association
Cardiovascular Medicine
Cardiology
TBX1 Loss‑of‑function Mutation Contributes to Congenital Conotruncal Defects
Experimental and Therapeutic Medicine
Medicine
Cancer Research
Immunology
Microbiology
Cardiac Alpha- And Beta-Myosin Heavy Chain Genes Are Organized in Tandem.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
A Novel Mutation in the TM6 Domain of GABBR2 Leads to a Rett-Like Phenotype
Annals of Neurology
Neurology
