INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH. (2021)
Attributed to:
Exosomal protein deficiencies: how abnormal RNA metabolism results in childhood-onset neurological diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/brain/awab133
PubMed Identifier: 33792664
Publication URI: http://europepmc.org/abstract/MED/33792664
Type: Journal Article/Review
Volume: 144
Parent Publication: Brain : a journal of neurology
Issue: 8
ISSN: 0006-8950