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

Full text not available from this repository.

Item Type:	Article
Faculty \ School:	Faculty of Medicine and Health Sciences > Norwich Medical School
UEA Research Groups:	Faculty of Medicine and Health Sciences > Research Groups > Medicine (former - to 2013) Faculty of Medicine and Health Sciences > Research Groups > Musculoskeletal Medicine
Depositing User:	EPrints Services
Date Deposited:	25 Nov 2010 11:13
Last Modified:	16 Jun 2023 00:04
URI:	https://ueaeprints.uea.ac.uk/id/eprint/15312
DOI:	10.1111/j.1399-0004.2007.00887.x

Actions (login required)

View Item