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Fatal familial insomnia: the first account in a family of Chinese descent.
Sian D SD Spacey, Manuela M Pastore, Barbara B McGillivray, Jonathan J Fleming, Pierluigi P Gambetti and Howard H Feldman
Arch Neurol 61(1):122-5 (2004)
PMID 14732629
Fatal familial insomnia (FFI) is an autosomal dominant disease linked to a mutation in the prion protein gene. Fatal familial insomnia is characterized by sleep disturbance and loss of neurons, with gliosis in the thalamic nuclei.
DOI: 10.1001/archneur.61.1.122
Version: za2963e q8za4 q8zb8 q8zcb q8zdd q8zef q8zfd q8zg1
DOI: 10.1001/archneur.61.1.122
Version: za2963e q8za4 q8zb8 q8zcb q8zdd q8zef q8zfd q8zg1