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Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants (2020)

First Author: Neuray Caroline

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

Type: Journal Article/Review

Volume: 143

Parent Publication: BRAIN

ISSN: 0006-8950