Antithrombin gene mutation 5356–5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin α-helix D molecular pathology

✍ Scribed by M. Steiner; B. Steiner; A. Rolfs; M. Wangnick; C. Burstein; M. Freund; P. Schuff-Werner

• Publisher: Springer
• Year: 2005
• Tongue: English
• Weight: 46 KB
• Volume: 84
• Category: Article
• ISSN: 0939-5555
• DOI: 10.1007/s00277-005-1045-1