Homozygous TAF8 mutation in a patient with intellectual disability results in undetectable TAF8 protein, but preserved RNA polymerase II transcription. (2018)
Attributed to:
BrisSynBio: Bristol Centre for Synthetic Biology
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/hmg/ddy126
PubMed Identifier: 29648665
Publication URI: http://europepmc.org/abstract/MED/29648665
Type: Journal Article/Review
Volume: 27
Parent Publication: Human molecular genetics
Issue: 12
ISSN: 0964-6906