Prion protein (PRNP) genotypes in frontotemporal lobar degeneration syndromes

Ann Neurol. 2006 Nov;60(5):616. doi: 10.1002/ana.20931.

Authors

Jonathan D Rohrer¹, Simon Mead², Rohani Omar¹, Mark Poulter², Jason D Warren¹, John Collinge², Martin N Rossor¹

Affiliations

¹ Dementia Research Centre, Department of Neurodegenerative Diseases, Institute of Neurology, University College London, National Hospital for Neurology and Neurosurgery, London, United Kingdom.
² MRC Prion Unit, Department of Neurodegenerative Diseases, Institute of Neurology, University College London, National Hospital for Neurology and Neurosurgery, London, United Kingdom.

PMID: 16969862
DOI: 10.1002/ana.20931

No abstract available

Publication types

Letter
Comment

MeSH terms

Codon / genetics
DNA Mutational Analysis
Dementia / genetics*
Genotype
Humans
Point Mutation / genetics*
Polymorphism, Genetic / genetics
Prion Proteins
Prions / genetics*
Syndrome

Substances

Codon
PRNP protein, human
Prion Proteins
Prions

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