Literature DB >> 18811698

A novel genetic locus for benign familial infantile seizures maps to chromosome 1p36.12-p35.1.

H Y Li, N Li, H Jiang, L Shen, J F Guo, R X Zhang, K Xia, Q Pan, X H Zi, B S Tang.   

Abstract

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Year:  2008        PMID： 18811698     DOI： 10.1111/j.1399-0004.2008.01092.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  2 in total

1.  PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.

Authors:  Sarah E Heron; Bronwyn E Grinton; Sara Kivity; Zaid Afawi; Sameer M Zuberi; James N Hughes; Clair Pridmore; Bree L Hodgson; Xenia Iona; Lynette G Sadleir; James Pelekanos; Eric Herlenius; Hadassa Goldberg-Stern; Haim Bassan; Eric Haan; Amos D Korczyn; Alison E Gardner; Mark A Corbett; Jozef Gécz; Paul Q Thomas; John C Mulley; Samuel F Berkovic; Ingrid E Scheffer; Leanne M Dibbens
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

2.  Genetic variations and associated pathophysiology in the management of epilepsy.

Authors:  John C Mulley; Leanne M Dibbens
Journal:  Appl Clin Genet       Date:  2011-08-08
  2 in total

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