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Your search keyword '"Neerman-Arbez M"' showing total 3 results

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3 results on '"Neerman-Arbez M"'

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1. Homozygosity for a Thr575Met missense mutation in the catalytic domain associated with factor XI deficiency.

2. Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.

3. Severe factor XI deficiency in a Lebanese family: identification of a novel missense mutation (Trp501Cys) in the catalytic domain.

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