Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome. (2015)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.7554/elife.06602
PubMed Identifier: 26026149
Publication URI: http://europepmc.org/abstract/MED/26026149
Type: Journal Article/Review
Volume: 4
Parent Publication: eLife
ISSN: 2050-084X