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Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis (2014)

First Author: Martin H

Attributed to: University of Oxford Big Data Institute: Development & dissemination of efficient analysis methods for large, complex, heterogeneous clinical datasets funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddu030

PubMed Identifier: 24463883

Publication URI: http://europepmc.org/abstract/MED/24463883

Type: Journal Article/Review

Parent Publication: Human Molecular Genetics

Issue: 12

ISSN: 0964-6906