Targeted Excision of VCP R155H Mutation by Cre-LoxPTechnology as a Promising Therapeutic Strategy for Valosin-Containing Protein Disease
Author:
Affiliation:
1. Division of Genetics and Genomics Medicine, Department of Pediatrics, University of California–Irvine, Irvine, CA 92697.
2. Department of Pathology and Laboratory Medicine, University of California–Irvine, Irvine, CA 92697.
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical),Pharmacology,Genetics,Applied Microbiology and Biotechnology,Molecular Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/hgtb.2014.096
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1. Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone
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3. Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes
4. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
5. Clinical studies in familial VCP myopathy associated with Paget disease of bone and frontotemporal dementia
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