Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities. (2009)
Attributed to:
Molecular genetics of Meckel-Gruber syndrome, and functional characterization of meckelin and MKS1
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2009.01.011
PubMed Identifier: 19200523
Publication URI: http://europepmc.org/abstract/MED/19200523
Type: Journal Article/Review
Volume: 84
Parent Publication: American journal of human genetics
Issue: 2
ISSN: 0002-9297