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Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome. (2020)

First Author: Ramsbottom SA

Attributed to: Models, modifiers and novel treatments of Joubert syndrome funded by MRC

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