Associated Papers
Genetics and functional genomics of multiple sclerosis.
Kim W et al.
Seminars in Immunopathology, 2022
Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations.
van de Putte R et al.
Plos One, 2019
Low-Frequency and Rare-Coding Variation Contributes to Multiple Sclerosis Risk.
Unknown Author
Cell, 2018
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