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Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy. (2016)

First Author: Madeo M

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2016.04.008

PubMed Identifier: 27236917

Publication URI: http://europepmc.org/abstract/MED/27236917

Type: Journal Article/Review

Volume: 98

Parent Publication: American journal of human genetics

Issue: 6

ISSN: 0002-9297