Associated Papers
Missense BICD2 variants in fetuses with congenital arthrogryposis and pterygia.
Masuda L et al.
Human Genome Variation, 2024
39183348 (PubMed )
Supplement: 41439_2024_290_MOESM1_ESM.pdf
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes.
Fan Q et al.
Nature Communications, 2023
37696869 (PubMed )
Supplement: 41467_2023_41256_MOESM3_ESM.xlsx › Supplementary_Data_9
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