Associated Papers
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Supplement: 41598_2025_6096_MOESM1_ESM.xlsx › S2
The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency.
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Unique Features of Germline Variation in Five Egyptian Familial Breast Cancer Families Revealed by Exome Sequencing.
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28076423 (PubMed )
Supplement: pone.0167581.s005.xlsx › 24_Caucasian_controls
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