Novel variants broaden the phenotypic spectrum of PLEKHG5-associated neuropathies. (2021)
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/10.1111/ene.14649
PubMed Identifier: 33220101
Publication URI: http://europepmc.org/abstract/MED/33220101
Type: Journal Article/Review
Volume: 28
Parent Publication: European journal of neurology
Issue: 4
ISSN: 1351-5101