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New Data from Zunyi Medical University Illuminate Findings in Factor VII Deficiency (Hereditary Coagulation Factor Vii Deficiency Caused By Novel Compound Heterozygous Mutations C.572-1g>a > a and C.1037a>c > C In a Chinese Pedigree).
- Source :
- Hematology Week; 12/6/2024, p330-330, 1p
- Publication Year :
- 2024
-
Abstract
- A recent study conducted at Zunyi Medical University in Guizhou, China, focused on hereditary coagulation Factor VII deficiency, a rare bleeding disorder. The research identified novel compound heterozygous mutations in the F7 gene, shedding light on the genetic mechanisms underlying the condition. The findings not only contribute to understanding FVII deficiency but also offer potential insights for future diagnostic and therapeutic strategies. This peer-reviewed study provides valuable information for researchers and healthcare professionals interested in inherited blood coagulation disorders. [Extracted from the article]
Details
- Language :
- English
- ISSN :
- 1543673X
- Database :
- Complementary Index
- Journal :
- Hematology Week
- Publication Type :
- Periodical
- Accession number :
- 181149372