A Nonsense Mutation in FGA g.3807C→T (p.R159X) Causes Afibrinogenaemia in the Homozygous Form

Publisher: Karger

E-ISSN: 1421-9662|121|4|216-217

ISSN: 0001-5792

Source: Acta Haematologica, Vol.121, Iss.4, 2009-05, pp. : 216-217

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