Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome. (2020)
Attributed to:
Newcastle Confidence in Concept 2017
funded by
UKRI
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1073/pnas.1912602117
PubMed Identifier: 31879347
Publication URI: http://europepmc.org/abstract/MED/31879347
Type: Journal Article/Review
Volume: 117
Parent Publication: Proceedings of the National Academy of Sciences of the United States of America
Issue: 2
ISSN: 0027-8424