Evaluation of CACNA1H in European patients with childhood absence epilepsy-Reference-Cited by-同舟云学术

Evaluation of CACNA1H in European patients with childhood absence epilepsy

Published:2006-05 Issue:2 Volume:69 Page:177-181
ISSN:0920-1211
Container-title:Epilepsy Research
language:en
Short-container-title:Epilepsy Research

Author:

Chioza Barry,Everett Kate,Aschauer Harald,Brouwer Oebele,Callenbach Petra,Covanis Athanasios,Dulac Olivier,Durner Martina,Eeg-Olofsson Orvar,Feucht Martha,Friis Mogens,Heils Armin,Kjeldsen Marianne,Larsson Katrin,Lehesjoki Anna-Elina,Nabbout Rima,Olsson Ingrid,Sander Thomas,Sirén Auli,Robinson Robert,Rees Michele,Gardiner R. Mark

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference21 articles.

1. Association between genetic variation of CACNA1H and childhood absence epilepsy;Chen;Ann. Neurol.,2003

2. T-type calcium channel gene alpha (1G) is not associated with childhood absence epilepsy in the Chinese Han population;Chen;Neurosci. Lett.,2003

3. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families;Corder;Science,1993

4. Childhood absence epilepsy: genes, channels, neurons and networks;Crunelli;Nat. Rev. Neurosci.,2002

5. Block of cloned human T-type calcium channels by succinimide antiepileptic drugs;Gomora;Mol. Pharmacol.,2001

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