Genotype-Phenotype Correlation in the Long-QT Syndrome

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Circulation

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

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Nature Genetics

Mendelian DisorderGenetic DisorderGeneticsDegenerative DiseaseDisease Gene Identification +1

Hypertrophic Cardiomyopathy

Pascale Richard, Philippe Charron, Lucie Carrier, +13

Circulation

Autologous skeletal myoblast transplantation for severe postinfarction left ventricular dysfunction

Philippe Menasché, Albert Hagège, Jean‐Thomas Vilquin, +11

Journal of the American College of Cardiology

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy, +9

Nature Genetics

Novel MutationChannelopathiesCardiomyopathyMolecular PhysiologyCardiac Muscle +8

Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

A. Leclerc, Xu Zhang, Haluk Topaloğlu, +8

Nature Genetics

Rare DiseasesLaminin α2–Chain GeneDevelopmental BiologyGenetic DisorderMedicine +6

Three myosin heavy-chain isozymes appear sequentially in rat muscle development

Robert G. Whalen, Susan M. Sell, Gillian Butler‐Browne, +3

Nature

Muscle PhysiologyRat Muscle DevelopmentDevelopmental BiologyMolecular PhysiologyMuscle Function +10

Myosin isoenzyme redistribution in chronic heart overload

Anne‐Marie Lompré, Ketty Schwartz, Anne d’Albis, +3

Nature

Cardiac MuscleCardiomyopathyHeart FailureMedicinePhysiology +4

Cardiac myosin binding protein–C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy

Gisèle Bonne, Lucie Carrier, J. Bercovici, +12

Nature Genetics

Cardiac MuscleCardiomyopathyHeart FailureCardiac MyosinCardiovascular Disease +8

Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

Marina Raffaele di Barletta, Enzo Ricci, Giuliana Galluzzi, +15

The American Journal of Human Genetics

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsDegenerative Disease +5