Associated Papers
Rare variants in MYH15 modify amyotrophic lateral sclerosis risk.
Kim H et al.
Human Molecular Genetics, 2019
Loss of human ICOSL results in combined immunodeficiency.
Roussel L et al.
The Journal of Experimental Medicine, 2018
30498080 (PubMed )
Supplement: JEM_20180668_TableS1.xlsx › SR5064319_min_10_reads_annotate
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