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Mutation analysis of the lamin A/C gene (<i>LMNA</i>) among patients with different cardiomuscular phenotypes

Michal Vytopil, Sara Benedetti, Enzo Ricci, Giuliana Galluzzi, Antonio Dello Russo, Luciano Merlini, Giuseppe Boriani, Maria Adelaide Gallina, Lucía Morandi, Luisa Politano,

Journal of Medical Genetics · 2003 · 113 citations · 21 references

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21

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

, , +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

, , +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

, , +5

Nuclear lamin A/C R482Q mutation in Canadian kindreds with Dunnigan-type familial partial lipodystrophy

Henian Cao · Human Molecular Genetics · 2000 · 657 citations · Full text

, , +15

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984.

Mary Codd, D. Sugrue, Bernard J. Gersh et al. · Circulation · 1989 · 642 citations

, , +7