Title: | Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy - double trouble as an explanation for an atypical phenotype |
Journal : | Neuromuscular disorders : NMD, 18, 11 |
Authors: | Rudnik Schoneborn S ; Weis J ; Kress W ; Häusler M ; Zerres K |
Material Type: | Article |
Publication Date: | 2008 |
Size: | p. 881-885 |
Languages: | English |
Keywords : | associated diseases ; Becker muscular dystrophy ; case studies ; creatine kinase ; D4Z4 locus ; DYS gene ; facioscapulohumeral muscular dystrophy ; histochemistry ; molecular biology ; muscle biopsies ; photographies ; skeletal muscle ; splicing ; Western blot |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/pubmed/18684626?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum |