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Properties of lamin A mutants found in Emery-Dreifuss muscular dystrophy, cardiomyopathy and Dunnigan-type partial lipodystrophy
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Complex formation between lamin A and the retinoblastoma gene product: Identification of the domain on lamin A required for its interaction
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LMNA, encoding lamin A/C, is mutated in partial lipodystrophy
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Shackleton, S., Lloyd, D.J., Jackson, S.N., Evans, R., Niermeijer, M.F., Singh, B.M., Schmidt, H., Brabant, G., Kumar, S., Durrington, RN., Gregory, S., O'Rahilly, S. and Trembath, R.C. (2000) LMNA, encoding lamin A/C, is mutated in partial lipodystrophy. Nat. Genet. 24, 153-156
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Crystal structure of the human lamin A coil 2B dimer: Implications for the head-to-tail association of nuclear lamins
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Proteins that bind A-type lamins: Integrating isolated clues
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