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Comment on Connolly AM, et al. Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin alpha2-deficient mice (Neuromuscul Disord 2001;11:703-712).

AuthorsGerta Vrbová
JournalNeuromuscular disorders : NMD (Neuromuscul Disord) Vol. 12 Issue 6 Pg. 608-9; author reply 609 (Aug 2002) ISSN: 0960-8966 [Print] England
PMID12117488 (Publication Type: Comment, Letter)
Chemical References
  • Cytoskeletal Proteins
  • Dystrophin
  • Laminin
  • Membrane Proteins
  • Muscle Proteins
  • Utrn protein, mouse
  • Utrophin
  • laminin alpha 2
Topics
  • Animals
  • Cytoskeletal Proteins (deficiency, genetics)
  • Disease Models, Animal
  • Dystrophin (deficiency, genetics)
  • Laminin (deficiency, genetics)
  • Membrane Proteins (deficiency, genetics)
  • Mice
  • Mice, Knockout
  • Muscle Fatigue
  • Muscle Proteins (deficiency, genetics)
  • Muscular Dystrophies (genetics, metabolism)
  • Mutation
  • Phenotype
  • Reproducibility of Results
  • Utrophin

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