Molecular analysis of severe factor XI deficiency in three Italian patients
Author:
Publisher
Wiley
Subject
Genetics(clinical),Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2516.2011.02576.x/fullpdf
Reference9 articles.
1. Identification of a novel mutation in a non-Jewish factor XI deficient kindred;Alhaq;Br J Haematol,1999
2. Nonsense-mediated mRNA decay in health and disease;Frischmeyer;Hum Mol Genet,1999
3. Characterization of seven novel mutations causing factor XI deficiency;Zucker;Haematologica,2007
4. Characterisation of five factor XI mutations;Mitchell;Thromb Haemost,2007
5. Eleven novel mutations in non-Jewish factor XI deficient kindreds detected by SSCP with heteroduplex analysis followed by sequencing;Bolton-Maggs;J Thromb Haemost,2003
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Detection and Gene Mutation Analysis of Three Variations in Two Unrelated Chinese Hereditary Coagulation Factor XI Deficiency Families;Acta Haematologica;2022
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