Title: | Hereditary myosin myopathies |
Journal : | Neuromuscular disorders : NMD, 17, 5 |
Authors: | Oldfors A |
Material Type: | Article |
Publication Date: | 2007 |
Size: | p. 355-367 |
Languages: | English |
Keywords : | actin ; arthrogryposis ; associated diseases ; autosomal dominant hyaline body myopathy ; dilated cardiomyopathy ; genetic mutations ; histochemistry ; hypertrophic cardiomyopathy ; immunohistochemistry ; Laing distal myopathy ; loss of ambulation ; molecular genetics ; muscle biopsies ; muscle contractures ; muscle hypertrophy ; muscle weakness ; MYH2 gene ; MYH7 gene ; myogenesis ; myosin heavy chain ; photographies ; physiopathology ; progressive external ophtalmoplegia ; protein structure ; reviews ; skeletal muscle |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=17434305&query_hl=5&itool=pubmed_docsum |