Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature.
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| Title: | Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature. |
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| Authors: | Zdziarska, Joanna1 (AUTHOR) jzdziarska@su.krakow.pl, Wypasek, Ewa2 (AUTHOR), Iwaniec, Teresa1 (AUTHOR), Vilar, Rui3 (AUTHOR), Neerman‐Arbez, Marguerite4 (AUTHOR), Undas, Anetta5 (AUTHOR) |
| Source: | Haemophilia. Jan2021, Vol. 27 Issue 1, p26-32. 7p. 1 Color Photograph, 2 Charts. |
| Database: | Academic Search Ultimate |
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