Mutation of POC1B in a severe syndromic retinal ciliopathy. (2014)
Attributed to:
Investigating Pix protein function in microtubule-related processes
funded by
BBSRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/humu.22618
PubMed Identifier: 25044745
Publication URI: http://europepmc.org/abstract/MED/25044745
Type: Journal Article/Review
Volume: 35
Parent Publication: Human mutation
Issue: 10
ISSN: 1059-7794