Severe Dejerine-Sottas disease with respiratory failure and dysmorphic features in association with a PMP22 point mutation and a 3q23 microdeletion. (2012)

First Author: Voermans NC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1111/j.1529-8027.2012.00402.x

PubMed Identifier: 22734911

Publication URI: http://europepmc.org/abstract/MED/22734911

Type: Journal Article/Review

Volume: 17

Parent Publication: Journal of the peripheral nervous system : JPNS

Issue: 2

ISSN: 1085-9489