APA

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. (20080104). Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. : Clinical genetics.

Chicago

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 and Kimonis V E. 20080104. Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. : Clinical genetics.

Harvard

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. and Kimonis V. E. (20080104). Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. : Clinical genetics.

MLA

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 and Kimonis V E. Novel VCP mutations in inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia. : Clinical genetics. 20080104.