Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes [1]

Annals of Neurology

Volumn 60, Issue 5, 2006, Pages 616-

  Rohrer, Jonathan D ^a   Mead, Simon ^a   Omar, Rohani ^a   Poulter, Mark ^a   Warren, Jason D ^a   Collinge, John ^a   Rossor, Martin N ^a  

^a NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

APHASIA; BRAIN DEGENERATION; CODON; CORTICOBASAL DEGENERATION; CREUTZFELDT JAKOB DISEASE; DISEASE ASSOCIATION; FRONTOTEMPORAL DEMENTIA; FRONTOTEMPORAL LOBAR DEGENERATION; GENE; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MOTOR NEURON DISEASE; PRION DISEASE; PRIORITY JOURNAL; PRNP GENE; PROTEIN POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED KINGDOM;

CODON; DEMENTIA; DNA MUTATIONAL ANALYSIS; GENOTYPE; HUMANS; POINT MUTATION; POLYMORPHISM, GENETIC; PRIONS; SYNDROME;

EID: 33845296159     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.20931     Document Type: Letter

References (4)

1. Collinge J. Prion diseases of humans and animals: their causes and molecular basis. Annu Rev Neurosci 2001;24:519-550.
2. Li X, Rowland LP, Mitsumoto H, et al. Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia. Ann Neurol 2005;58:858-864.
3. Mead S, Mahal SP, Beck J, et al. Sporadic but not variant - Creutzfeldt-Jakob disease is associated with polymorphisms upstream of PRNP exon 1. Am J Hum Genet 2001;69:1225-1235.
4. Neary D, Snowden JS, Gustafson L, et al. Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria. Neurology 1998;51:1546-1554.