Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger–Huët anomaly)

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

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

Gisèle Bonne, Marina Raffaele di Barletta, Shaïda Varnous et al. · Nature Genetics · 1999 · 1.3K citations

Life Sciences, Genetics, Molecular Genetics +7

LMNA, encoding lamin A/C, is mutated in partial lipodystrophy

Sue Shackleton, David J. Lloyd, Stephen N.J. Jackson et al. · Nature Genetics · 2000 · 701 citations

Life Sciences, Genetics, Molecular Biology +5

Essential Roles for<i>Caenorhabditis elegans</i>Lamin Gene in Nuclear Organization, Cell Cycle Progression, and Spatial Organization of Nuclear Pore Complexes

Jun Liu, Tom Rolef Ben-Shahar, Dieter Riemer et al. · Molecular Biology of the Cell · 2000 · 409 citations

Life Sciences, Biology, Genetics +17

Mutations in the Δ7-sterol reductase gene in patients with the Smith–Lemli–Opitz syndrome

Barbara U. Fitzky, Martina Witsch‐Baumgartner, Martin Erdel et al. · Proceedings of the National Academy of Sciences · 1998 · 388 citations

Life Sciences, Genetics, Molecular Genetics +17