Whole exome sequencing in familial Multiple Sclerosis - EGA European Genome-Phenome Archive

Study

Whole exome sequencing in familial Multiple Sclerosis

Study ID	Alternative Stable ID	Type
EGAS00001004204		Other

Study Description

The purpose of the study is to determine whether variants of genes are associated with greater risk of Multiple Sclerosis (MS). We used whole-exome sequencing in 138 individuals from 23 families including at least 2 members with MS. We compare patients with MS, patients with other autoimmune diseases (AID), and unaffected individuals.

Study Datasets 1 dataset.

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Dataset ID	Description	Technology	Samples
EGAD00001005952	Familial Multiple Sclerosis study dataset, including variant calling files from 138 samples with three different phenotypes: Multiple Sclerosis (MS), other Autoimmune Diseases (AID) and unaffected individuals. Familial Multiple Sclerosis study dataset, including variant calling files from 138 samples with three different phenotypes: Multiple Sclerosis (MS), other Autoimmune Diseases (AID) and unaffected individuals.		138

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