Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia-Reference-Cited by-同舟云学术

Genotype-phenotype studies of VCP-associated inclusion body myopathy with Paget disease of bone and/or frontotemporal dementia

Published:2012-10-04 Issue:5 Volume:83 Page:422-431
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Mehta SG,Khare M¹,Ramani R¹,Watts GDJ²,Simon M,Osann KE³,Donkervoort S¹,Dec E¹,Nalbandian A¹,Platt J,Pasquali M⁴,Wang A⁵,Mozaffar T⁵,Smith CD⁶,Kimonis VE¹

Affiliation:

1. Division of Genetics and Metabolism, Department of Pediatrics; University of California; Irvine; CA; USA

2. Biomedical Research Center; University of East Anglia; Norwich; Norfolk; UK

3. Division of Hematology/Oncology, Department of Medicine; University of California; Irvine; CA; USA

4. Department of Pathology, School of Medicine; University of Utah; Salt Lake City; UT; USA

5. ALS and Neuromuscular Center; University of California; Irvine; CA; USA

6. Department of Neurology and Sanders-Brown Center on Aging; University of Kentucky; Lexington; KY; USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference45 articles.

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2. Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes;Watts;Neuromuscul Disord,2003

3. Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia;Kovach;Mol Genet Metabol,2001

4. Kimonis V Donkervoort S Watts G GeneTests (www.genetests.org) and University of Washington, Seattle

5. The multiple faces of valosin-containing protein-associated diseases: inclusion body myopathy with Paget's disease of bone, frontotemporal dementia, and amyotrophic lateral sclerosis;Nalbandian;J Mol Neurosci,2011

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