A novel NGF mutation clarifies the molecular mechanism and extends the phenotypic spectrum of the HSAN5 neuropathy. (2011)

First Author: Carvalho OP


No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1136/jmg.2010.081455

PubMed Identifier: 20978020

Publication URI: http://europepmc.org/abstract/MED/20978020

Type: Journal Article/Review

Volume: 48

Parent Publication: Journal of medical genetics

Issue: 2

ISSN: 0022-2593