Associated Papers
Genetics of frontotemporal dementia in China.
Jiang Y et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2021
A novel VCP mutation as the cause of atypical IBMPFD in a Chinese family.
Gu JM et al.
Bone, 2013
A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.
Djamshidian A et al.
Muscle & Nerve, 2009
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