Anar, B.

patient mutation family protein dementia study x syndrome hair roots family history frontotemporal dementia frontotemporal fxr 2p disease brain syndrome parkinsonism supranuclear palsy history expression relative nucleus neurology control fxr proteins onset antibody frontotemporal lobar degeneration fmrpi 304n x patients motor neuron disease palsy supranuclear fmrp expression genet autosomal diagnosis export cytoplasm progranulin fxr 1p family members pathology genetic analysis neurol sclerosis inclusion hippocampal sclerosis localization --------------- degeneration fxr 2pmut report -43 fmrpi group blood hippocampal individual substantia nigra netherland treatment result transfected lobar pgrn mutations antibody test defect number nucleolu tremor grn mutations -------------- oostra retardation chromosome female fmrp 34a 2pmut domain