Concepedia

Mandibuloacral Dysplasia Is Caused by a Mutation in LMNA-Encoding Lamin A/C

Giuseppe Novelli, Antoine Muchir, Federica Sangiuolo, A. Leclerc, Maria Rosaria D’Apice, Catherine Massart, Francesca Capon, Paolo Sbraccia, Massimo Federici, Renato Lauro,

The American Journal of Human Genetics · 2002 · 535 citations · 25 references

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25

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

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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

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

, , +17