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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.
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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  Data: 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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  Data: <searchLink fieldCode="JN" term="%22Haemophilia%22">Haemophilia</searchLink>. Jan2021, Vol. 27 Issue 1, p26-32. 7p. 1 Color Photograph, 2 Charts.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=148454457
RecordInfo BibRecord:
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      – Type: doi
        Value: 10.1111/hae.14211
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      – Code: eng
        Text: English
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        PageCount: 7
        StartPage: 26
    Titles:
      – TitleFull: 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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            NameFull: Zdziarska, Joanna
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            NameFull: Wypasek, Ewa
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            NameFull: Iwaniec, Teresa
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            NameFull: Vilar, Rui
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            NameFull: Neerman‐Arbez, Marguerite
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            NameFull: Undas, Anetta
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            – D: 01
              M: 01
              Text: Jan2021
              Type: published
              Y: 2021
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              Value: 27
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