Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes-Reference-Cited by-同舟云学术

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Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes

Published:2018-02-07 Issue: Volume:9 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Dunn Paul,Albury Cassie L.,Maksemous Neven,Benton Miles C.,Sutherland Heidi G.,Smith Robert A.,Haupt Larisa M.,Griffiths Lyn R.

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference116 articles.

1. Analysis of rare copy number variation in absence epilepsies;Addis;Neurol Genet.,2016

2. Analyzing and minimizing PCR amplification bias in Illumina sequencing libraries;Aird;Genome Biol.,2011

3. A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield;Ankala;Ann. Neurol.,2015

4. The risks of seizure disorders among relatives of patients with childhood onset epilepsy;Annegers;Neurology,1982

5. Deep sequencing multi-gene panel analysis is a useful first-tier test with a high diagnostic yield and broad mutation spectrum detection in childhood epilepsy;Aradhya;J. Neurol. Sci.,2017

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