Targeted sequencing and identification of genetic variants in sporadic inclusion body myositis

Author:

Weihl Conrad C.,Baloh Robert H.,Lee Youjin,Chou Tsui-Fen,Pittman Sara K.,Lopate Glenn,Allred Peggy,Jockel-Balsarotti Jennifer,Pestronk Alan,Harms Matthew B.

Funder

Ultragenyx Pharmaceuticals, Novato CA

NIH

Muscular Dystrophy Association

Myositis Association

Hope Center for Neurological Disorders

Burroughs Wellcome Fund

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference47 articles.

1. Sporadic inclusion body myositis: possible pathogenesis inferred from biomarkers;Weihl;Curr Opin Neurol,2010

2. A 12-year follow-up in sporadic inclusion body myositis: an end stage with major disabilities;Cox;Brain,2011

3. Long-term observational study of sporadic inclusion body myositis;Benveniste;Brain,2011

4. Light and electron microscopic localization of beta-amyloid protein in muscle biopsies of patients with inclusion-body myositis;Askanas;Am J Pathol,1992

5. Twisted tubulofilaments of inclusion body myositis muscle resemble paired helical filaments of Alzheimer brain and contain hyperphosphorylated tau;Askanas;Am J Pathol,1994

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