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PMID: 14575910 Published · ppublish English Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis.

Journal of neuroimmunology ·Vol. 143 ·No. 1-2 ·2003-10-00 ·Pages 25-30

Hensiek AE, Roxburgh R, Smilie B, Coraddu F, Akesson E, Holmans P, Sawcer SJ, Compston DA

Abstract

In 1996, we reported the results of a linkage genome screen based on 129 UK multiple sclerosis multiplex families, together with follow-up typing of interesting regions in a second set of families. We have now completed screening the remainder of the genome in this second set of United Kingdom families by typing 242 microsatellite markers. These data have been analysed together with those previously published, resulting in the largest currently available whole genome linkage dataset from a single population in multiple sclerosis. Four new regions of potential linkage (chromosomes 10p, 11p, 19p, 20p) not previously described were identified. In the combined analysis of all 226 families, a total of five regions of suggestive linkage are seen (chromosomes 1p, 6p, 14q, 17q, Xq), where only one would have been expected to occur by chance alone.

MeSH Terms
Alleles Electrophoresis, Polyacrylamide Gel Female Genetic Linkage Genetic Markers Genetic Predisposition to Disease Genetic Testing/methods Genome, Human Genotype Histocompatibility Testing Humans Male Microsatellite Repeats Multiple Sclerosis/epidemiology,genetics,immunology Polymerase Chain Reaction Siblings United Kingdom/epidemiology
Chemicals
Genetic Markers
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Hensiek A E
Neurology Unit, Addenbrooke's Hospital, University of Cambridge, Hills Road, Cambridge CB2 2QQ, UK.
Roxburgh R
Smilie B
Coraddu F
Akesson E
Holmans P
Sawcer S J
Compston D A S
Article Info
Journal
Journal of neuroimmunology
Abbr.
J Neuroimmunol
ISSN
0165-5728
Published
2003-10-00
Pages
25-30
Language
English
Region
Netherlands
NLM ID
8109498
Subset
IM
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