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SCN1B-linked early infantile developmental and epileptic encephalopathy. (2019)

First Author: Aeby A

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/10.1002/acn3.50921

PubMed Identifier: 31709768

Publication URI: http://europepmc.org/abstract/MED/31709768

Type: Journal Article/Review

Volume: 6

Parent Publication: Annals of clinical and translational neurology

Issue: 12

ISSN: 2328-9503