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C9ORF72 and UBQLN2 mutations are causes of amyotrophic lateral sclerosis in New Zealand: a genetic and pathologic study using banked human brain tissue. (2017)

First Author: Scotter EL

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