Author:
Castaldo Giuseppe,D'Argenio Valeria,Nardiello Paola,Zarrilli Federica,Sanna Veronica,Rocino Angiola,Coppola Antonio,Di Minno Giovanni,Salvatore Francesco
Abstract
AbstractHaemophilia A is the most common inherited bleeding disorder caused by defects in theClin Chem Lab Med 2007;45:450–61.
Subject
Biochemistry, medical,Clinical Biochemistry,General Medicine
Reference119 articles.
1. Cag layan SH FV Leiden ) and mutations in the factor molecular insights Article in press - uncorrected proof V gene : incidence in deep venous thrombosis and hemophilia A patients;Berber;Haemophilia Haematol,2003
2. Identification of factor VIII gene mutations in patients with haemophilia A : mutation analysis by inversion screening and multiplex PCR and CSGE and molecular modeling of novel missense substitutions;Jayandharan;Haemophilia,2005
3. Haemophilia : strategies for carrier detection and prenatal diagnosis;Peake;Bull World Health Organ,1993
4. Molecular cloning of a cDNA encoding human antihaemophilic factor;Toole;Nature,1984
5. Perinatal management of neonates with haemophilia;Kulkarni;Br Haematol,2001
Cited by
46 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