G. Watts

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

D. Drachman, A. Kaminska, C. Weihl, 2007, Clinical genetics.

Familial lipoprotein lipase (LPL) deficiency: A catalogue of LPL gene mutations identified in 20 patients from the UK, Sweden, and Italy

P. Talmud, H. Lithell, D. Muller, 1997, Human mutation.

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

J. Platt, M. Pasquali, K. Osann, 2013, Clinical genetics.