Inherited Creutzfeldt-Jakob disease in a British family associated with a novel 144 base pair insertion of the prion protein gene.

Author:

Nicholl D,Windl O,de Silva R,Sawcer S,Dempster M,Ironside J W,Estibeiro J P,Yuill G M,Lathe R,Will R G

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference24 articles.

1. A retrospective study of Creutzfeldt-Jakob disease in England and Wales 1970-1979 II: epidemiology;Will, R.G.; Matthews, W.B.; Smith, P.G.; Hudson, C.;J Neurol Neurosurg Psychiatry,1986

2. The familial occurrence of Creutzfeldt-Jakob disease and Alzheimer's disease;Masters, C.L.; Gajdusek, D.C.; Gibbs, C.J.;Brain,1981

3. The molecular genetics of human transmissible spongiform encephalopathy;Goldfarb, L.G.; Brown, P.; Gajdusek, D.C.,1992

4. Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Straussler syndrome;Kitamoto, T.; Ohta, M.; Doh-ura, K.; Hitoshi, S.; Terao, Y.; Tateishi, J.;Biochem Biophys Research Commun,1993

5. Dementia associated with a 216 base pair insertion in the prion protein gene;Duchen, L.W.; Poulter, M.; Harding, A.E.;Brain,1993

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