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