KCNB1 Mutations in Epileptic Encephalopathy

J Gordon Millichap; John J Millichap

doi:10.15844/pedneurbriefs-28-12-2

KCNB1 Mutations in Epileptic Encephalopathy

Pediatric Neurology Briefs

Volume 28 (2014): Issue 12

By: J Gordon Millichap and John J Millichap

Open Access

|Dec 2014

Abstract

Researchers at Scripps Research Institute, San Diego, and other centers in California; Johns Hopkins, Baltimore; Vanderbilt University, TN; and Northwestern University Feinberg School of Medicine, Chicago, IL; searched for de novo mutations in a family with a sporadic case of epileptic encephalopathy.

References

Torkamani A Bersell K Jorge BS Bjork RL Jr Friedman JR Bloss CS De novo KCNB1 mutations in epileptic encephalopathy Ann Neurol 2014 Oct 76 4 529 40 10.1002/ana.24263 25164438
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Veeramah KR Johnstone L Karafet TM Wolf D Sprissler R Salogiannis J Exome sequencing reveals new causal mutations in children with epileptic encephalopathies Epilepsia 2013 Jul 54 7 1270 81 10.1111/epi.12201 23647072
Open DOI Search in Google Scholar Back to article
Torkamani A Bersell K Jorge BS Bjork RL Jr Friedman JR Bloss CS De novo KCNB1 mutations in epileptic encephalopathy Ann Neurol 2014 Oct 76 4 529 40 10.1002/ana.24263 25164438
Open DOI Search in Google Scholar Back to article

Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-28-12-2 | Journal eISSN: 2166-6482

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Language: English

Page range: 90 - 90

Published on: Dec 1, 2014

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Neurology,

Pediatrics,

Child Development,

Nervous System Diseases,

Brain Diseases

© 2014 J Gordon Millichap, John J Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 28 (2014): Issue 12