Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2020 |
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| Erschienen: |
2020 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:193 |
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| Enthalten in: |
Thrombosis research - 193(2020) vom: 05. Sept., Seite 5-8 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Vilar, Rui [VerfasserIn] |
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| Links: |
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| Themen: |
9001-32-5 |
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| Anmerkungen: |
Date Completed 17.06.2021 Date Revised 31.05.2022 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1016/j.thromres.2020.05.040 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM310775329 |
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| 245 | 1 | 0 | |a Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A |
| 264 | 1 | |c 2020 | |
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| 500 | |a Date Revised 31.05.2022 | ||
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| 650 | 4 | |a Letter | |
| 650 | 4 | |a Research Support, Non-U.S. Gov't | |
| 650 | 4 | |a Bleeding | |
| 650 | 4 | |a Congenital fibrinogen disorders | |
| 650 | 4 | |a FGA | |
| 650 | 4 | |a Fibrinogen | |
| 650 | 4 | |a Hypofibrinogenemia | |
| 650 | 4 | |a Mutation | |
| 650 | 7 | |a FGA protein, human |2 NLM | |
| 650 | 7 | |a Fibrinogen |2 NLM | |
| 650 | 7 | |a 9001-32-5 |2 NLM | |
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| 700 | 1 | |a Mourey, Guillaume |e verfasserin |4 aut | |
| 700 | 1 | |a Neerman-Arbez, Marguerite |e verfasserin |4 aut | |
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