Novel insights into PORCN mutations, associated phenotypes and pathophysiological aspects. (2022)
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/10.1186/s13023-021-02068-w
PubMed Identifier: 35101074
Publication URI: http://europepmc.org/abstract/MED/35101074
Type: Journal Article/Review
Volume: 17
Parent Publication: Orphanet journal of rare diseases
Issue: 1
ISSN: 1750-1172