Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype–phenotype relationship-Reference-Cited by-同舟云学术

Factor XI gene variants in factor XI-deficient patients of Southern Italy: identification of a novel mutation and genotype–phenotype relationship

Published:2017-11-09 Issue:1 Volume:4 Page:
ISSN:2054-345X
Container-title:Human Genome Variation
language:en
Short-container-title:Hum Genome Var

Author:

Tiscia Giovanni L^ORCID,Favuzzi Giovanni,Lupone Maria R,Cappucci Filomena,Schiavulli Michele,Mirabelli Valentina^ORCID,D’Andrea Giovanna,Chinni Elena,Giuliani Nicola,Caliandro Rocco,Grandone Elvira

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

Link

http://www.nature.com/articles/hgv201743.pdf

Reference40 articles.

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3. Gomez K, Bolton-Maggs P . Factor XI deficiency. Haemophilia 2008; 14: 1183–1189.

4. Mulder R, Wiewel-Verschueren S, Meijer K, Mulder AB . Identification of a novel factor XI gene mutational event in a Dutch Caucasian family with inherited factor XI deficiency. Thromb Haemost 2013; 109: 1183–1185.

5. Seligsohn U . Factor XI deficiency in humans. J Thromb Haemost 2009; 7: 84–87.

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