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