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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. (2021)

First Author: Van Rheenen W

Attributed to: Using Next Generation Sequencing to Unravel the Pathogenesis of Sporadic Inclusion Body Myositis - The International IBM Consortium Genetic Study funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41588-021-00973-1

PubMed Identifier: 34873335

Publication URI: http://europepmc.org/abstract/MED/34873335

Type: Journal Article/Review

Volume: 53

Parent Publication: Nature genetics

Issue: 12

ISSN: 1061-4036