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Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in Aicardi-Goutières syndrome. (2013)

First Author: Rice GI

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