Title: | Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis |
Journal : | Neurobiology of aging, 47 |
Authors: | Gang Q, Author ; Bettencourt C ; Machado PM ; Brady S ; Holton JL ; Pittman AM ; Hughes D ; Healy E ; Parton M ; Hilton-Jones D ; Shieh PB ; Needham M ; Liang C ; Zanoteli E ; de Camargo LV ; de Paepe B ; De Bleecker J ; Shaibani A ; Ripolone M ; Violano R ; Moggio M ; Barohn RJ ; Dimachkie MM ; Mora M ; Mantegazza R ; Zanotti S ; Singleton AB ; Hanna MG ; Houlden H |
Material Type: | Article |
Publication Date: | 2016 |
Size: | p 218.e1 |
Languages: | English |
Keywords : | cohort studies ; genetic mutations ; genetic susceptibility ; inclusion body myositis ; muscle histopathology ; protein structure ; risk factors ; sequencing ; SQSTM1 gene ; VCP gene |
Keywords: | Genetic risk factor;SQSTM1;Sporadic inclusion body myositis;VCP;sIBM; |
Pubmed / DOI : | DOI : 10.1016/j.neurobiolaging.2016.07.024 / Pubmed : 27594680 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/27594680 |