A nonsense mutation in FGA g.3807C-->T (p.R159X) causes afibrinogenaemia in the homozygous form. [electronic resource]

By: Contributor(s): Producer: 20090825Description: 216-7 p. digitalISSN:
  • 1421-9662
Subject(s): Online resources: In: Acta haematologica vol. 121
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Publication Type: Case Reports; Journal Article

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