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Genetic variation at 16q24.2 is associated with small vesse..:
Traylor, Matthew
;
Malik, Rainer
;
Nalls, Mike A
...
https://www.repository.cam.ac.uk/handle/1810/262766. , 2017
Link:
https://www.repository.cam.ac.uk/handle/1810/262766
RT Journal T1
Genetic variation at 16q24.2 is associated with small vessel stroke
UL https://suche.suub.uni-bremen.de/peid=base-ftunivcam:oai:www.repository.cam.ac.uk:1810_262766&Exemplar=1&LAN=DE A1 Traylor, Matthew A1 Malik, Rainer A1 Nalls, Mike A A1 Cotlarciuc, Ioana A1 Radmanesh, Farid A1 Thorleifsson, Gudmar A1 Hanscombe, Ken B A1 Langefeld, Carl A1 Saleheen, Danish A1 Rost, Natalia S A1 Yet, Idil A1 Spector, Tim D A1 Bell, Jordana T A1 Hannon, Eilis A1 Mill, Jonathan A1 Chauhan, Ganesh A1 Debette, Stephanie A1 Bis, Joshua C A1 Longstreth, WT A1 Ikram, M Arfan A1 Launer, Lenore J A1 Seshadri, Sudha A1 METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium A1 Hamilton-Bruce, Monica Anne A1 Jimenez-Conde, Jordi A1 Cole, John W A1 Schmidt, Reinhold A1 Słowik, Agnieszka A1 Lemmens, Robin A1 Lindgren, Arne A1 Melander, Olle A1 Grewal, Raji P A1 Sacco, Ralph L A1 Rundek, Tatjana A1 Rexrode, Kathryn A1 Arnett, Donna K A1 Johnson, Julie A A1 Benavente, Oscar R A1 Wasssertheil-Smoller, Sylvia A1 Lee, Jin-Moo A1 Pulit, Sara L A1 Wong, Quenna A1 Rich, Stephen S A1 de Bakker, Paul IW A1 McArdle, Patrick F A1 Woo, Daniel A1 Anderson, Christopher D A1 Xu, Huichun A1 Heitsch, Laura A1 Fornage, Myriam A1 Jern, Christina A1 Stefansson, Kari A1 Thorsteinsdottir, Unnur A1 Gretarsdottir, Solveig A1 Lewis, Cathryn M A1 Sharma, Pankaj A1 Sudlow, Cathie LM A1 Rothwell, Peter M A1 Boncoraglio, Giorgio B A1 Thijs, Vincent A1 Levi, Chris A1 Meschia, James F A1 Rosand, Jonathan A1 Kittner, Steven J A1 Mitchell, Braxton D A1 Dichgans, Martin A1 Worrall, Bradford B A1 Markus, Hugh S A1 International Stroke Genetics Consortium PB Wiley; http://dx.doi.org/10.1002/ana.24840; Ann Neurol YR 2017 K1 Adult K1 Aged K1 80 and over K1 Cerebral Small Vessel Diseases K1 Chromosomes K1 Human K1 Pair 16 K1 Female K1 Genetic Loci K1 Genetic Variation K1 Genome-Wide Association Study K1 Humans K1 Male K1 Middle Aged K1 Stroke K1 Lacunar K1 Zinc Fingers JF https://www.repository.cam.ac.uk/handle/1810/262766 LK http://dx.doi.org/https://www.repository.cam.ac.uk/handle/1810/262766 DO https://www.repository.cam.ac.uk/handle/1810/262766 SF ELIB - SuUB Bremen
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