CareLit · DOI-Nachweis · Zeitschrift für Orthopädie und Unfallchirurgie
Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations
DOI 10.1055/a-2086-4328
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Nachweis in CareLit
Autor:innenChen, Y.; Zhang, K.; Jin, Y.; Zeng, M.; Jia, K.; Yang, L.; Wang, M.
ZeitschriftZeitschrift für Orthopädie und Unfallchirurgie
Ausgabe06/2023
Jahrgang / SeitenJg. 43 · S. 418 bis 425
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Abstract-Vorschau
Abstract Objective This study aims to provide a preliminary discussion of the molecular basis of FV deficiency caused by compound heterozygous mutations in two Chinese families. Methods Relative coagulation index was measured by the one-stage clotting method and the FV:Ag was measured by ELISA. All exons and flanking regions of the F5 gene were amplified by PCR and directly sequenced. ClustalX-2.1-win was used to an…
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Zitierempfehlung
Chen, Y.; Zhang, K.; Jin, Y.; Zeng, M.; Jia, K.; Yang, L.; Wang, M (2023) Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations. Zeitschrift für Orthopädie und Unfallchirurgie, 43 (06), 418 bis 425. https://doi.org/10.1055/a-2086-4328
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