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The variable phenotypes of KCNQ-related epilepsy

  • Published:2014-07-22 Issue:9 Volume:55 Page:e99-e105
  • ISSN:0013-9580
  • Container-title:Epilepsia
  • language:en
  • Short-container-title:Epilepsia

Author:

Allen Nicholas M.1,Mannion Maria1,Conroy Judith2,Lynch Sally A.23,Shahwan Amre1,Lynch Bryan1,King Mary D.12

Affiliation:

1. Department of Paediatric Neurology & Clinical Neurophysiology; Children's University Hospital; Dublin Ireland

2. Academic Centre on Rare Diseases; School of Medicine and Medical Science; University College; Dublin Ireland

3. Department of Clinical Genetics; Children's University Hospital; Temple St. Dublin Ireland

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference24 articles.

1. Genetic testing in benign familial epilepsies of the first year of life: clinical and diagnostic significance;Zara;Epilepsia,2013

2. Genetics of epilepsy syndromes starting in the first year of life;Deprez;Neurology,2009

3. Benign familial neonatal convulsions caused by mutation in KCNQ3, exon 6: a European case;Fister;Eur J Paediatr Neurol,2013

4. Contiguous deletion of KCNQ2 and CHRNA4 may cause a different disorder from benign familial neonatal seizures;Pascual;Epilepsy Behav Case Rep,2013

5. Benign familial neonatal convulsions: always benign?;Steinlein;Epilepsy Res,2007

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