Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. (2018)
Attributed to:
MICA: MRC Centre for Neuromuscular Diseases
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2018.10.002
PubMed Identifier: 30388405
Publication URI: http://europepmc.org/abstract/MED/30388405
Type: Journal Article/Review
Volume: 103
Parent Publication: American journal of human genetics
Issue: 5
ISSN: 0002-9297