Nuclear envelope proteins and neuromuscular diseases - Östlund, Cecilia; Worman, Howard J. (Muscle & nerve, 2003)
Keywords: Animals; Biological and medical sciences; cardiomyopathy; Charcot-Marie-Tooth disease; Cytoskeleton - genetics; Cytoskeleton - metabolism; Cytoskeleton - pathology; Diseases of striated muscles. Neuromuscular diseases; emerin; Emery-Dreifuss muscular dystrophy; Humans; lamin; Lamin Type A - genetics; Lamin Type A - metabolism; limb-girdle muscular dystrophy; lipodystrophy; Medical sciences; Membrane Proteins - genetics; Membrane Proteins - metabolism; Muscle, Skeletal - metabolism; Muscle, Skeletal - pathology; muscular dystrophy; Mutation - genetics; Neurology; Neuromuscular Diseases - genetics; Neuromuscular Diseases - metabolism; Neuromuscular Diseases - pathology; Nuclear Envelope - genetics; Nuclear Envelope - metabolism; Nuclear Proteins; Thymopoietins - genetics; Thymopoietins - metabolism; Cell culture; Animal model; Emery-Dreifuss muscular dystrophy; Cardiovascular disease; Review; Myocardial disease; Nuclear envelope; limb-girdle muscular dystrophy; muscular dystrophy; Emery Dreifuss muscular dystrophy; Gene; Heart disease; Charcot-Marie-Tooth disease; Degenerative disease; Coat protein; cardiomyopathy; Nervous system diseases; Neuromuscular diseases; lamin; Genetic disease; emerin; Congestive hypertrophic cardiomyopathy; Charcot Marie Tooth disease; Central nervous system disease; Limb girdle muscular dystrophy; Lipodystrophy; Adipose tissue disorders; Mutation; Spinal cord disease