Novel homozygous fibrinogen Aα chain truncation causes severe afibrinogenemia with life threatening complications in a two-year-old boy
Thrombosis research.
2013 Oct ;
132 (4) :
490-2.
[epub] 20130901
Language English Country United States Media print-electronic
Document type Case Reports, Letter, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid24050829
PubMed
24050829
DOI
10.1016/j.thromres.2013.08.022
PII: S0049-3848(13)00377-0
Knihovny.cz E-resources
- MeSH
- Afibrinogenemia blood genetics MeSH
- Fibrinogen genetics metabolism MeSH
- Fibrinogens, Abnormal genetics metabolism MeSH
- Homozygote MeSH
- Humans MeSH
- Child, Preschool MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Child, Preschool MeSH
- Publication type
- Letter MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- fibrinogen Aalpha MeSH Browser
- Fibrinogen MeSH
- Fibrinogens, Abnormal MeSH
References provided by Crossref.org
International journal of molecular sciences.
2021 Dec 23 ;
23 (1) :
.
[epub] 20211223
