The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders. (2017)
Attributed to:
Using transcriptomics to transform the diagnosis and understanding of inherited adult neurological disorders
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awx155
PubMed Identifier: 28899015
Publication URI: http://europepmc.org/abstract/MED/28899015
Type: Journal Article/Review
Volume: 140
Parent Publication: Brain : a journal of neurology
Issue: 8
ISSN: 0006-8950