Muscle MRI findings in patients with an apparently exclusive cardiac phenotype due to a novel LMNA gene mutation

Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease

Diane Fatkin, Calum A. MacRae, Takeshi Sasaki et al. · New England Journal of Medicine · 1999 · 1.4K citations · Full text

Medicine, Genetics, Molecular Genetics +17

cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins.

D Z Fisher, Nilabh Chaudhary, Günter Blobel · Proceedings of the National Academy of Sciences · 1986 · 715 citations

Life Sciences, Biochemistry, Molecular Biology +17

Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

Fan Lin, Howard J. Worman · Journal of Biological Chemistry · 1993 · 624 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene

Gisèle Bonne, Eugenio Mercuri, Antoine Muchir et al. · Annals of Neurology · 2000 · 491 citations

Medicine, Genetics, Molecular Genetics +14

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

Marina Raffaele di Barletta, Enzo Ricci, Giuliana Galluzzi et al. · The American Journal of Human Genetics · 2000 · 411 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11