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Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk / Erratum


Mitrovič, Mitja; Patsopoulos, Nikolaos A; et al; Martin, Roland; Sospedra, Mireia; Jelcic, Ilijas (2019). Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk / Erratum. Cell, 178(1):262.

Abstract

Erratum in Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk.
International Multiple Sclerosis Genetics Consortium. Electronic address: chris.cotsapas@yale.edu; International Multiple Sclerosis Genetics Consortium. Cell. 2020 Jan 23;180(2):403. doi: 10.1016/j.cell.2020.01.002. PMID: 31978348 Free PMC article.

Abstract

Erratum in Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk.
International Multiple Sclerosis Genetics Consortium. Electronic address: chris.cotsapas@yale.edu; International Multiple Sclerosis Genetics Consortium. Cell. 2020 Jan 23;180(2):403. doi: 10.1016/j.cell.2020.01.002. PMID: 31978348 Free PMC article.

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Additional indexing

Contributors:International Multiple Sclerosis Genetics Consortium
Item Type:Journal Article, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Clinic for Neurology
Dewey Decimal Classification:610 Medicine & health
Scopus Subject Areas:Life Sciences > General Biochemistry, Genetics and Molecular Biology
Uncontrolled Keywords:General Biochemistry, Genetics and Molecular Biology
Language:English
Date:1 June 2019
Deposited On:17 Dec 2019 12:03
Last Modified:12 Sep 2020 03:39
Publisher:Cell Press (Elsevier)
ISSN:0092-8674
OA Status:Hybrid
Free access at:PubMed ID. An embargo period may apply.
Publisher DOI:https://doi.org/10.1016/j.cell.2019.06.016
Related URLs:https://www.zora.uzh.ch/id/eprint/159332/
PubMed ID:31251915

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