Polymorphism at codon 129 of the prion protein gene is not associated with sporadic AD

Neurology

Volumn 55, Issue 4, 2000, Pages 593-595

  Combarros, O ^a   Sanchez Guerra M ^a   Llorca, J ^b   Alvarez Arcaya, A ^a   Berciano, J ^a   Pena N ^c   Fernandez Viadero C ^c  

^a HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

^b UNIVERSITY OF CANTABRIA   (Spain)

^c Consejería de Sanidad ^*  (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE; PRION PROTEIN; VALINE;

ADULT; AGED; ALZHEIMER DISEASE; ARTICLE; CODON; COGNITION; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENETIC POLYMORPHISM; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PRIORITY JOURNAL;

EID: 0033845154     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.55.4.593     Document Type: Article

References (8)

1. Chaperoning brain diseases
2. Prions
3. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt-Jakob disease
4. Codon 129 prion protein genotype and sporadic Creutzfeldt-Jakob disease
5. Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease
6. Genetics of prions
7. Polymorphism of the prion protein is associated with cognitive impairment in the elderly. The EVA study
8. Clinical diagnosis of Alzheimer's disease: Report of the NINCDA-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease