Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A
| Affiliation auteurs | !!!! Error affiliation !!!! |
| Titre | Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A |
| Type de publication | Journal Article |
| Year of Publication | 2020 |
| Auteurs | Vilar R, Casini A, Fournel A, Mourey G, Neerman-Arbez M |
| Journal | THROMBOSIS RESEARCH |
| Volume | 193 |
| Pagination | 5-8 |
| Date Published | SEP |
| Type of Article | Letter |
| ISSN | 0049-3848 |
| Mots-clés | bleeding, Congenital fibrinogen disorders, FGA, Fibrinogen, Hypofibrinogenemia, mutation |
| DOI | 10.1016/j.thromres.2020.05.040 |