Identification of a novel amino acid deletion mutation and a very rare single nucleotide variant in a Japanese family with type I antithrombin deficiency

✍ Scribed by Kan Katayama; Natsuko Hashimoto; Yuki Tanaka; Tetsuo Ozawa; Yoshiharu Emi; Takeshi Ikeda; Miyuki Katayama; Shinsuke Nomura; Isao Kitajima; Takeshi Nakano; Tsuneo Imanaka

• Book ID: 116913153
• Publisher: Elsevier Science
• Year: 2005
• Tongue: English
• Weight: 204 KB
• Volume: 116
• Category: Article
• ISSN: 0049-3848
• DOI: 10.1016/j.thromres.2004.12.004