Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis
Nat Genet
.
2010 Jun;42(6):469-70; author reply 470-1.
doi: 10.1038/ng0610-469.
Authors
International Multiple Sclerosis Genetics Consortium (IMSGC)
;
David R Booth
,
Robert N Heard
,
Graeme J Stewart
,
Mathew Cox
,
Rodney J Scott
,
Jeannette Lechner-Scott
,
An Goris
,
Rita Dobosi
,
Bénédicte Dubois
,
Janna Saarela
,
Virpi Leppä
,
Leena Peltonen
,
Tuula Pirttila
,
Isabelle Cournu-Rebeix
,
Bertrand Fontaine
,
Laura Bergamaschi
,
Sandra D'Alfonso
,
Maurizio Leone
,
Aslaug R Lorentzen
,
Hanne F Harbo
,
Elisabeth G Celius
,
Anne Spurkland
,
Jenny Link
,
Ingrid Kockum
,
Tomas Olsson
,
Jan Hillert
,
Maria Ban
,
Amie Baker
,
Anu Kemppinen
,
Stephen Sawcer
,
Alastair Compston
,
Neil P Robertson
,
Philip L De Jager
,
David A Hafler
,
Lisa F Barcellos
,
Adrian J Ivinson
,
Jacob L McCauley
,
Margaret A Pericak-Vance
,
Jorge R Oksenberg
,
Stephen L Hauser
,
David Sexton
,
Jonathan Haines
PMID:
20502484
PMCID:
PMC3109873
DOI:
10.1038/ng0610-469
No abstract available
Publication types
Letter
Comment
MeSH terms
Genetic Predisposition to Disease
Genetic Variation*
Humans
Kinesins / genetics*
Multiple Sclerosis / genetics*
Substances
KIF1B protein, human
Kinesins
Grants and funding
WT_/Wellcome Trust/United Kingdom
R01 NS049477/NS/NINDS NIH HHS/United States
R01 NS049477-01A1/NS/NINDS NIH HHS/United States