Nalaganje...
A novel fibrinogen mutation: FGA g. 3057 C > T (p. Arg104 > Cys) impairs fibrinogen secretion
BACKGROUND: Abnormal fibrinogens can be caused by clinically silent hereditary mutations. A new case was detected accidentally in an 11-year-old girl when routine pre-operative coagulation tests were performed for nasal turbinate surgery. METHODS: The fibrinogen genes FGA, FGG and FGB were sequenced...
Shranjeno v:
| izdano v: | BMC Hematol |
|---|---|
| Main Authors: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2017
|
| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5741905/ https://ncbi.nlm.nih.gov/pubmed/29299315 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12878-017-0086-8 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|