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
Parent Publication: The American Journal of Human Genetics
Issue: 5
ISSN: 0002-9297