Please use this identifier to cite or link to this item:
doi:10.22028/D291-43631
Title: | The FGG c.952G>A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral infarction: a case report |
Author(s): | Ying, Anna Zhou, Yuanlin Wang, Chunyue Wang, Tao Zhang, Xuan Wang, Shanshan Ke, Shaofa Bao, Yuyan Liu, Yang Wang, Feng |
Language: | English |
Title: | Frontiers in neurology |
Volume: | 15 |
Publisher/Platform: | Frontiers |
Year of Publication: | 2024 |
Free key words: | FGG gene c.952G>A congenital dysfibrinogenemia cerebral infarction fibrinogen |
DDC notations: | 620 Engineering and machine engineering |
Publikation type: | Journal Article |
Abstract: | Congenital dysfibrinogenemia (CD) is a rare hereditary coagulation disorder resulting from mutations in fibrinogen genes. CD primarily presents with bleeding symptoms, but it can also lead to thrombotic events, including ischemic stroke. |
DOI of the first publication: | 10.3389/fneur.2024.1272802 |
URL of the first publication: | https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2024.1272802/full |
Link to this record: | urn:nbn:de:bsz:291--ds-436317 hdl:20.500.11880/39091 http://dx.doi.org/10.22028/D291-43631 |
ISSN: | 1664-2295 |
Date of registration: | 2-Dec-2024 |
Faculty: | NT - Naturwissenschaftlich- Technische Fakultät |
Department: | NT - Materialwissenschaft und Werkstofftechnik |
Professorship: | NT - Prof. Dr. Volker Presser |
Collections: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
Files for this record:
File | Description | Size | Format | |
---|---|---|---|---|
fneur-15-1272802.pdf | 436,91 kB | Adobe PDF | View/Open |
This item is licensed under a Creative Commons License