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The Genetics of Multiple Sclerosis
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Alastair Compston
Veröffentlicht/Copyright:
1. Juni 2005
Abstract
Classical genetic studies involving the analysis of pedigrees and recurrence risk within families have defined the extent to which genetic factors contribute to the aetiology of multiple sclerosis. Limited progress has been made in identifying the number and topography of genetic loci contributing to susceptibility through molecular investigation either of candidate genes or the whole genome using microsatellite and single nucleotide polymorphisms.
:
Published Online: 2005-06-01
Published in Print: 2000-02-05
Copyright © 2000 by Walter de Gruyter GmbH & Co. KG
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Artikel in diesem Heft
- IFCC WorldLab '99
- Markers of Endothelial Dysfunction
- Standardization and Quality Control of PCR Analyses
- Histochemical and Immunocytochemical Approaches to the Study of Oxidative Stress
- Sniffing out the Truth: Clinical Diagnosis Using the Electronic Nose
- Oncogenes and Thyroid Cancer
- Paraneoplastic Syndromes of the Nervous System
- Genetic Modifying Factors in β-Thalassemia
- The Genetics of Multiple Sclerosis
- Near-Infrared Reflectance Spectroscopy for Noninvasive Monitoring of Metabolites
- Ribozyme Gene Therapy for Autosomal Dominant Retinal Disease
- Oxidized Lipoproteins and Endothelium
- Experiences with External Quality Assessment (EQA) in Molecular Diagnostics in Clinical Laboratories in Germany
- Unravelling Genetic Data by Arrayed Primer Extension
- Evaluation of RNA Isolation Methods and Reference Genes for RT-PCR Analyses of Rare Target RNA
- IFCC WorldLab Daily News
