Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia.
Watts, G. D. J.; Thomasova, D.; Ramdeen, S. K.; Fulchiero, E. C.; Mehta, S. G.; Drachman, D. A.; Weihl, C. C.; Jamrozik, Z.; Kwiecinski, H.; Kaminska, A.; Kimonis, V. E.; Clinical Genetics, 2007, vol. 72, issue 5, p 420, ISSN 00099163. ISBN 00099163.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef