Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia

Watts, GD, Thomasova, D, Ramdeen, SK, Fulchiero, EC, Mehta, SG, Drachman, DA, Weihl, CC, Jamrozik, Z, Kwiecinski, H, Kaminska, A and Kimonis, VE (2007) Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. Clinical Genetics, 72 (5). pp. 420-426. ISSN 1399-0004

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Item Type: Article
Faculty \ School: Faculty of Medicine and Health Sciences > Norwich Medical School
Depositing User: EPrints Services
Date Deposited: 25 Nov 2010 11:13
Last Modified: 30 Apr 2020 23:45
URI: https://ueaeprints.uea.ac.uk/id/eprint/15312
DOI: 10.1111/j.1399-0004.2007.00887.x

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