Title: | Thin filament proteins mutations associated with skeletal myopathies : defective regulation of muscle contraction |
Journal : | Journal of molecular medicine, 86, 11 |
Authors: | Ochala J |
Material Type: | Article |
Publication Date: | 11/2008 |
Size: | p. 1197-1204 |
Languages: | English |
Keywords : | ACTA1 gene ; actin ; alpha-tropomyosin ; arthrogryposis ; beta-tropomyosin related cap disease ; congenital fiber-type disproportion myopathy selenoprotein related ; congenital myopathy ; contractility ; core and rod myopathy ; genetic mutations ; modes of action ; muscle biopsies ; muscle contraction ; muscle wasting ; muscle weakness ; NEB gene ; nebulin ; quality of life ; review article ; rod myopathy ; skeletal muscle ; TNNI2 gene ; TNNT1 gene ; TPM2 gene ; TPM3 gene ; troponin |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/pubmed/18574571?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum |