Associated Papers
The landscape of rare genetic variants in familial Waldenström macroglobulinemia.
Pemov A et al.
Blood Neoplasia, 2024
39036705 (PubMed )
Supplement: BNEO_NEO-2023-000111-mmc4.xlsx › Supplementary_Table_4
Exome sequencing in families with chronic central serous chorioretinopathy.
Schellevis RL et al.
Molecular Genetics & Genomic Medicine, 2019
30724488 (PubMed )
Supplement: MGG3-7-na-s005.xlsx › Family_17
Novel missense variants in the RNF213 gene from a European family with Moyamoya disease.
Gagunashvili AN et al.
Human Genome Variation, 2019
31645973 (PubMed )
Supplement: 41439_2019_66_MOESM1_ESM.pdf
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