Ontology highlight
ABSTRACT:
SUBMITTER: Zorina-Lichtenwalter K
PROVIDER: S-EPMC5828382 | biostudies-literature | 2018 Mar
REPOSITORIES: biostudies-literature
Zorina-Lichtenwalter Katerina K Parisien Marc M Diatchenko Luda L
Pain 20180301 3
Numerous studies have shown associations between genetic variants and neuropathic pain disorders. Rare monogenic disorders are caused by mutations of substantial effect size in a single gene, whereas common disorders are likely to have a contribution from multiple genetic variants of mild effect size, representing different biological pathways. In this review, we survey the reported genetic contributors to neuropathic pain and submit them for validation in a 150,000-participant sample of the U.K ...[more]