Simple and efficient identification of rare recessive pathologically important sequence variants from next generation exome sequence data. (2013)

First Author: Carr IM

Attributed to: Engineering Therapeutic Microbubbles funded by EPSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.22322

PubMed Identifier: 23554237

Publication URI: http://europepmc.org/abstract/MED/23554237

Type: Journal Article/Review

Volume: 34

Parent Publication: Human mutation

Issue: 7

ISSN: 1059-7794