Open Access Green as soon as Postprint is submitted to ZB.
Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease.
Brain 137:e295 (2014)
Publication type
Article: Journal article
Document type
Scientific Article
Keywords
Exome Sequencing Reveals; Deficiency
ISSN (print) / ISBN
0006-8950
e-ISSN
1460-2156
Journal
Brain: A Journal of Neurology
Quellenangaben
Volume: 137,
Issue: 9,
Article Number: e295
Publisher
Oxford University Press
Publishing Place
Oxford
Reviewing status
Peer reviewed
Institute(s)
Institute of Human Genetics (IHG)