Autosomal Recessive Keratoderma-Ichthyosis-Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen Modification. (2017)
Attributed to:
Super Resolution Imaging for Cell Biology and Neuroscience at UCL
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.jid.2016.12.010
PubMed Identifier: 28017832
Publication URI: http://europepmc.org/abstract/MED/28017832
Type: Journal Article/Review
Volume: 137
Parent Publication: The Journal of investigative dermatology
Issue: 4
ISSN: 0022-202X