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Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. (2019)

First Author: Bell S

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2019.03.022

PubMed Identifier: 31031012

Publication URI: http://europepmc.org/abstract/MED/31031012

Type: Journal Article/Review

Volume: 104

Parent Publication: American journal of human genetics

Issue: 5

ISSN: 0002-9297