Associated Papers
Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases.
Bhérer C et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
40791678 (PubMed )
Supplement: media-2.xlsx › Table_S12_ClinVar_PLP_variants
Novel Insights into Heterozygous Factor XIII Deficiency.
Dorgalaleh A
Seminars in Thrombosis and Hemostasis, 2024
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participants.
Stefanucci L et al.
Blood, 2023
37647632 (PubMed )
Supplement: BLOOD_BLD-2023-020118-mmc3.xlsx › ST3.4
Identification of a novel mutation in the factor XIII A subunit in a patient with inherited factor XIII deficiency.
Yan L et al.
International Journal of Hematology, 2023
Genetic landscape in coagulation factor XIII associated defects - Advances in coagulation and beyond.
Javed H et al.
Blood Reviews, 2023
Whole-exome mutational landscape of neuroendocrine carcinomas of the gallbladder.
Liu F et al.
Signal Transduction and Targeted Therapy, 2021
33563892 (PubMed )
Supplement: 41392_2020_412_MOESM16_ESM.xlsx › Supplementary_Table_S15
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