Candidate monogenic MS genes rare variant burden code

Zenodo (CERN European Organization for Nuclear Research) 2026 Open access

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Authors: Peter Juvan
DOI: 10.5281/zenodo.18586975
Cited by: 0

Abstract

Code used for burden analysis of the paper: "Monogenic causes for multiple sclerosis – a validation study"

Fields of Study & Subjects

Multiple Sclerosis Research Studies Genetic Associations and Epidemiology Genomics and Rare Diseases

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
10 February 2026
Language
EN