Article
Early-onset Alzheimers and cortical vision impairment in a woman with valosin-containing protein disease associated with 2 APOE ε4/APOE ε4 genotype.
Alzheimer disease and associated disorders - 1 Jan 2000
Shamirian Sharis, Nalbandian Angèle, Khare Manaswitha, Castellani Rudolph, Kim Ronald, Kimonis Virginia E
Abstract excerpt
Hereditary inclusion body myopathy is a heterogeneous group of disorders characterized by rimmed vacuoles and by the presence of filamentous cytoplasmic and intranuclear inclusions. Inclusion body myopathy with Paget disease of bone and frontotemporal dementia is a progressive autosomal dominant disorder associated with a mutation in valosin-containing protein (VCP) with typical onset of symptoms in the 30s. APOE...
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