Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease. (2012)

First Author: Johnson JO

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1093/brain/aws161

PubMed Identifier: 22740598

Publication URI: http://europepmc.org/abstract/MED/22740598

Type: Journal Article/Review

Volume: 135

Parent Publication: Brain : a journal of neurology

Issue: Pt 9

ISSN: 0006-8950