Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome. (2014)
Attributed to:
Nudc as a new molecular target to investigate the pathogenesis and treatment of skeletal ciliopathies.
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2014.10.007
PubMed Identifier: 25439728
Publication URI: http://europepmc.org/abstract/MED/25439728
Type: Journal Article/Review
Volume: 95
Parent Publication: American journal of human genetics
Issue: 5
ISSN: 0002-9297