Expanding the phenotype of the CDKL5 deficiency disorder: Are seizures mandatory? (2020)
Attributed to:
Chromosome maintenance and repair in health and disease
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1002/ajmg.a.61504
PubMed Identifier: 32034940
Publication URI: http://europepmc.org/abstract/MED/32034940
Type: Journal Article/Review
Volume: 182
Parent Publication: American journal of medical genetics. Part A
Issue: 5
ISSN: 1552-4825