Title: | Autosomal dominant nemaline myopathy caused by a novel alpha-tropomyosin 3 mutation |
Journal : | Journal of neurology, 257, 4 |
Authors: | Kiphuth IC ; Krause S ; Huttner HB ; Dekomien G ; Struffert T ; Schröder R |
Material Type: | Article |
Publication Date: | 2010 |
Size: | p. 658-660 |
Languages: | English |
Keywords : | alpha-tropomyosin ; autosomal dominant inheritance ; case studies ; genetic mutations ; Germany ; histochemistry ; molecular genetics ; muscle biopsies ; rod myopathy ; skeletal muscle ; TPM3 gene |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/pubmed/20012312 |
Pubmed / DOI : | DOI : 10.1007/s00415-009-5413-y |