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Intragenic DOK7 deletion detected by whole-genome sequencing in congenital myasthenic syndromes. (2017)

First Author: Azuma Y

Attributed to: New genomic approaches to explore the neurogenetic disease burden of consanguineous marriages in Turkey funded by Newton Fund

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1212/nxg.0000000000000152

PubMed Identifier: 28508085

Publication URI: http://europepmc.org/abstract/MED/28508085

Type: Journal Article/Review

Volume: 3

Parent Publication: Neurology. Genetics

Issue: 3

ISSN: 2376-7839