Autosomal Recessive Keratoderma-Ichthyosis-Deafness (ARKID) Syndrome Is Caused by VPS33B Mutations Affecting Rab Protein Interaction and Collagen Modification-Reference-Cited by-同舟云学术

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

Published:2017-04 Issue:4 Volume:137 Page:845-854
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Gruber Robert,Rogerson Clare,Windpassinger Christian,Banushi Blerida,Straatman-Iwanowska Anna,Hanley Joanna,Forneris Federico,Strohal Robert,Ulz Peter,Crumrine Debra,Menon Gopinathan K.,Blunder Stefan,Schmuth Matthias,Müller Thomas,Smith Holly,Mills Kevin,Kroisel Peter,Janecke Andreas R.,Gissen Paul

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

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