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Pseudo-exon activation caused by a deep-intronic mutation in the fibrinogen γ-chain gene as a novel mechanism for congenital afibrinogenaemia

✍ Scribed by Silvia Spena; Rosanna Asselta; Manuela Platé; Giancarlo Castaman; Stefano Duga; Maria Luisa Tenchini


Book ID
108675381
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
597 KB
Volume
139
Category
Article
ISSN
0007-1048

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