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Updated: Apr 15, 2026

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
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Identification of two novel missense mutations causing severe factor XIII deficiency
H Handrkova1,2, M Borhany3, V Schroeder1,2
1University Clinic of Haematology, Haemostasis Research Laboratory, University Hospital of Bern, Bern, Switzerland.
Summary
No abstract available in PubMed .
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