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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.2018.10.002

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