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Experimental Cell Research, ISSN 0014-4827, 2007, Volume 313, Issue 10, pp. 2121 - 2133
Mutations in genes encoding the intermediate filament nuclear lamins and associated proteins cause a wide spectrum of diseases sometimes called... 
Lamin | Lipodystrophy | Nuclear envelope | Intermediate filaments | Progeria | Muscular dystrophy | lamin | A-TYPE LAMINS | FAMILIAL PARTIAL LIPODYSTROPHY | INNER NUCLEAR-MEMBRANE | nuclear envelope | CELL BIOLOGY | progeria | PROGRESSIVE MULTIPLE-SCLEROSIS | muscular dystrophy | CAUSE AUTOSOMAL-DOMINANT | ONCOLOGY | INTERMEDIATE FILAMENT PROTEINS | HUTCHINSON-GILFORD-PROGERIA | DREIFUSS MUSCULAR-DYSTROPHY | LAMIN A/C GENE | BUSCHKE-OLLENDORFF-SYNDROME | intermediate filaments | lipodystrophy | Muscular Dystrophy, Emery-Dreifuss - genetics | Nuclear Matrix - genetics | Genetic Predisposition to Disease - genetics | Nuclear Envelope - genetics | Humans | Mutation - genetics | Lamins - chemistry | Syndrome | Nuclear Matrix - pathology | Lamins - genetics | Nuclear Envelope - metabolism | Muscular Dystrophy, Emery-Dreifuss - metabolism | Animals | Intermediate Filament Proteins - genetics | Lamins - metabolism | Muscular Dystrophy, Emery-Dreifuss - physiopathology | Nuclear Envelope - pathology | Active Transport, Cell Nucleus - genetics | Intermediate Filament Proteins - metabolism | Intermediate Filament Proteins - chemistry | Nuclear Matrix - metabolism | Proteins | Mutation | Cellular biology | Disease | MEMBRANE PROTEINS | DISEASES | FILAMENTS | THERAPY | GENES | PHENOTYPE | TEETH | AGING | MUTATIONS | SPECTRA | 60 APPLIED LIFE SCIENCES | SKELETON
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