C9ORF72 and UBQLN2 mutations are causes of amyotrophic lateral sclerosis in New Zealand: a genetic and pathologic study using banked human brain tissue. (2017)
Attributed to:
Exome sequencing in motor neuron disease: bioinformatic analyses and biological validation of novel variants
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1016/j.neurobiolaging.2016.06.019
PubMed Identifier: 27480424
Publication URI: http://europepmc.org/abstract/MED/27480424
Type: Journal Article/Review
Volume: 49
Parent Publication: Neurobiology of aging
ISSN: 0197-4580