Title: | Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis |
Journal : | Neuromuscular disorders : NMD, 25, 4 |
Authors: | Weihl CC ; Baloh RH ; Lee Y ; Chou TF ; Pittman SK ; Lopate G ; Allred P ; Jockel-Balsarotti J ; Pestronk A ; Harms MB |
Material Type: | Article |
Publication Date: | 2015 |
Size: | p 289 |
Languages: | English |
Keywords : | amyotrophic lateral sclerosis ; GNE myopathy ; inclusion body myositis ; myofibrillar myopathy ; physiopathology ; sequencing ; valosin containing protein related disease |
Keywords: | Amyotrophic lateral sclerosis;Hereditary inclusion body myopathy;Inclusion body myositis;Myofibrillar myopathy;VCP; |
Pubmed / DOI : | DOI : 10.1016/j.nmd.2014.12.009 / Pubmed : 25617006 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/25617006 |