Autosomal Recessive Keratoderma-Ichthyosis-Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen Modification. (2017)

First Author: Gruber R
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