Related content

Two novel factor X gene mutations in a Chinese family with factor X deficiency

By Au W.  

Annals of Hematology, Vol. 83, Iss. 5, 2004-05 ,pp. : 304-306

Springer Publishing Company

Access to resources Recommend Favorite

Five Novel and four recurrent point mutations in the antithrombin gene causing venous thrombosis

By Nagaizumi Keiko   Inaba Hiroshi   Amano Kagehiro   Suzuki Midori   Arai Morio   Fukutake Katsuyuki  

International Journal of Hematology, Vol. 78, Iss. 1, 2003-02 ,pp. : 79-83

Springer Publishing Company

Access to resources Recommend Favorite

Characterization of 11 New Cases of Leukocyte Adhesion Deficiency Type 1 with Seven Novel Mutations in the ITGB2 Gene

By Parvaneh Nima   Mamishi Setareh   Rezaei Amir   Rezaei Nima   Tamizifar Banafshe   Parvaneh Leila   Sherkat Roya   Ghalehbaghi Babak   Kashef Sara   Chavoshzadeh Zahra   Isaeian Anna   Ashrafi Farzaneh   Aghamohammadi Asghar  

Journal of Clinical Immunology, Vol. 30, Iss. 5, 2010-09 ,pp. : 756-760

Springer Publishing Company

Access to resources Recommend Favorite

Genetic analysis in nine unrelated Italian patients affected by OTC deficiency: detection of novel mutations in the OTC gene

By Bisanzi S.   Morrone A.   Donati M.A.   Pasquini E.   Spada M.   Strisciuglio P.   Parenti G.   Parini R.   Papadia F.   Zammarchi E.  

Molecular Genetics and Metabolism, Vol. 76, Iss. 2, 2002-06 ,pp. : 137-144

Academic Press

Access to resources Recommend Favorite

Molecular and Structural Analysis of Two Novel Mutations in a Patient with Mut^- Methylmalonyl-CoA Deficiency

By Benoist J-F.   Acquaviva C.   Callebaut I.   Guffon N.   Ogier de Baulny H.   Mornon J-P.   Porquet D.   Elion J.  

Molecular Genetics and Metabolism, Vol. 72, Iss. 2, 2001-02 ,pp. : 181-184

Academic Press

Access to resources Recommend Favorite