Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease. (2012)

First Author: Koutsis G


No abstract provided

Bibliographic Information

Digital Object Identifier:

PubMed Identifier: 22382358

Publication URI:

Type: Journal Article/Review

Volume: 135

Parent Publication: Brain : a journal of neurology

Issue: Pt 8

ISSN: 0006-8950