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.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
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.

Who archives the data?

There are no publications available