Title: | Mitochondrial processes are impaired in hereditary inclusion body myopathy |
Journal : | Human molecular genetics, 17, 23 |
Authors: | Eisenberg I ; Novershtern N ; Itzhaki Z ; Becker-Cohen M ; Sadeh M ; Willems PHGM ; Friedman N ; Koopman WJH ; Mitrani-Rosenbaum S |
Material Type: | Article |
Publication Date: | 2008 |
Size: | p. 3663-3674 |
Languages: | English |
Keywords : | cell cultures ; founder effect ; GNE gene ; inclusion body myopathy ; Jews ; messenger RNA ; microarrays ; mitochondria ; mitochondrial proteins ; modes of action ; molecular biology ; physiopathology ; sialic acid ; skeletal muscle |
Abstract: |
Accès au résumé PubMed / to PubMed abstract |
Lien associé : | http://www.ncbi.nlm.nih.gov/pubmed/18723858?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum |
Pubmed / DOI : | DOI : 10.1093/hmg/ddn261 |