Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis [Letter]

Booth, David R., Heard, Robert N., Stewart, Graeme J., Cox, Mathew, Scott, Rodney J., Lechner-Scott, Jeannette, Goris, An, Dobosi, Rita, Dubois, Bénédicte, Saarela, Janna, Leppä, Virpi, Peltonen, Leena, Pirttila, Tuula, Cournu-Rebeix, Isabelle, Fontaine, Bertrand, Bergamaschi, Laura, D'Alfonso, Sandra, Leone, Maurizio, Lorentzen, Åslaug R., Harbo, Hanne F., Celius, Elisabeth G., Spurkland, Anne, Link, Jenny, Kockum, Ingrid, Olsson, Tomas, Hillert, Jan, Ban, Maria, Baker, Amie, Kemppinen, Anu, Sawcer, Stephen, Compston, Alastair, Robertson, Neil ORCID: https://orcid.org/0000-0002-5409-4909, De Jager, Philip L., Hafler, David A., Barcellos, Lisa F., Ivinson, Adrian J., McCauley, Jacob L., Pericak-Vance, Margaret A., Oksenberg, Jorge R., Hauser, Stephen L., Sexton, David and Haines, Jonathan 2010. Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis [Letter]. Nature Genetics 42 (6) , pp. 469-470. 10.1038/ng0610-469

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Item Type:	Article
Date Type:	Publication
Status:	Published
Schools:	MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG) Medicine
Subjects:	Q Science > QH Natural history > QH426 Genetics R Medicine > R Medicine (General) R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
Publisher:	Nature Publishing Group
ISSN:	1061-4036
Last Modified:	19 Oct 2022 08:41
URI:	https://orca.cardiff.ac.uk/id/eprint/18720

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