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14. Diverse cell death pathways result from a single missense mutation in weaver mouse

16. Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease

19. INSOMNIA IN FAMILIAL CREUTZFELDT JAKOB DISEASE (FCJD), E200K, WITH THALAMIC INVOLVEMENT

28. Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

35. PRNP Mutation (G131V) Associated With Gerstmann-Sträussler-Scheinker Disease.

38. Unique cerebellar phenotype combining granule and Purkinje cell loss: Morphological evidence forweaver*pcd double mutant mice

41. Salivary androgen-binding protein variation in Mus and other rodents.

42. Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant.

43. GerstmannSträusslerScheinker disease II Neurofibrillary tangles and plaques with PrPamyloid coexist in an affected family

44. GerstmannSträusslerScheinker disease I Extending the clinical spectrum

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