📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia. (2019)

First Author: Gorman KM

Attributed to: MRC Centre for Neuropsychiatric Genetics and Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2019.03.005

PubMed Identifier: 30982612

Publication URI: http://europepmc.org/abstract/MED/30982612

Type: Journal Article/Review

Volume: 104

Parent Publication: American journal of human genetics

Issue: 5

ISSN: 0002-9297