Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy (2020)
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.2020.04.011
PubMed Identifier: 32409253
Publication URI: http://europepmc.org/abstract/MED/32409253
Type: Journal Article/Review
Parent Publication: Neurobiology of Aging
ISSN: 0197-4580