Format

Send to

Choose Destination
See comment in PubMed Commons below
Neurology. 2004 Aug 10;63(3):557-60.

Cortical malformations are associated with a rare polymorphism of cellular prion protein.

Author information

1
CIREP, de Cirurgia de Epilepsia, Departamento de Neurologia, Psiquiatria e Psicologia Médica, Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brazil. vmartins@ludwig.org.br

Erratum in

  • Neurology. 2007 Jul 24;69(4):414-6.

Abstract

Studies in animals lacking the cellular prion protein (PrP(c)) gene (Prnp) showed higher neuronal excitability in vitro and increased sensitivity to seizures in vivo. The authors previously reported a rare polymorphism at codon 171 (Asn-->Ser) of human Prnp to be associated with mesial temporal lobe epilepsy related to hippocampal sclerosis. They demonstrated that the same variant allele is also associated with symptomatic epilepsies related to different forms of malformations of cortical development.

PMID:
15304595
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire
    Loading ...
    Support Center