Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. (2018)

First Author: Ghosh SG
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.2018.07.010

PubMed Identifier: 30100084

Publication URI: http://europepmc.org/abstract/MED/30100084

Type: Journal Article/Review

Volume: 103

Parent Publication: American journal of human genetics

Issue: 3

ISSN: 0002-9297