Montagna, P.

patient mutation family parkinsonism disease protein fbxo 7 isoform figure syndrome brain davison parkin study hemangioblastoma analysis tumor fbxo 7 proteins neurol expression neurology seizure degeneration fbxo 7 protein region localization park 7 control recessive parkinson park 6 tract onset linkage table pallidal germline ppd /s cerebellar hemangioblastoma vhl gene activity t 22m t 22m mutation netherland park 7 region pallidopyramidal cerebellar chromosome neuron vhl disease lobe epilepsy dutch epilepsy marker autosomal isoform 1 dystonia suppressor parkin mutations fbxo 7 gene university isoform 2 antibody nucleus locus italian family history r 498x substantia nigra parkin gene spastic neurology vol 51 hippocampal department pseudobabinski system fbxo 7 transcripts pallidum f-box domain