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 SizeFormat 
fneur-15-1272802.pdf436,91 kBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons