Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies. (2023)
Attributed to:
MRC Strategic Award to establish an International Centre for Genomic Medicine in Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/braincomms/fcad222
PubMed Identifier: 37794925
Publication URI: http://europepmc.org/abstract/MED/37794925
Type: Journal Article/Review
Volume: 5
Parent Publication: Brain communications
Issue: 5
ISSN: 2632-1297