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Genetic analysis in FXI deficient patients from northwestern Italy: three novel and one recurrent mutation.

European journal of haematology - 1 Apr 2013

Bicocchi Maria Patrizia, Rosano Camillo, Acquila Maura

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PMID: 23305485
DOI: 10.1111/ejh.12072

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Genetic analysis in FXI deficient patients from northwestern Italy: three novel and one recurrent mutation.PMID 23305485Read ↗

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