Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndrome. (2013)
Attributed to:
Human Genetics Unit Senior Clinical Fellowship
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.22336
PubMed Identifier: 23592335
Publication URI: http://europepmc.org/abstract/MED/23592335
Type: Journal Article/Review
Volume: 34
Parent Publication: Human mutation
Issue: 8
ISSN: 1059-7794