Neuronal intranuclear inclusion disease is genetically heterogeneous. (2020)
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/10.1002/acn3.51151
PubMed Identifier: 32777174
Publication URI: http://europepmc.org/abstract/MED/32777174
Type: Journal Article/Review
Volume: 7
Parent Publication: Annals of clinical and translational neurology
Issue: 9
ISSN: 2328-9503