Author:
Khajoee Vahid,Ihara Kenji,Kira Ryutaro,Takemoto Megumi,Torisu Hiroyuki,Sakai Yasunari,Guanjun Jia,Hee Park Myoung,Tokunaga Katsushi,Hara Toshiro
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference28 articles.
1. Dib C, Faure S, Fizames C, Samon D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Lathrop M, Gyapay G, Morissette J, Weissenbach J (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152–154
2. Fukumori Y, Yoshimura K, Ohnoki S, Yamaguchi H, Akagaki Y, Inai S (1989) A high incidence of C9 deficiency among healthy blood donors in Osaka, Japan. Int Immunol 1:85–89
3. Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Mark S, Bernardi G, Lathrop M, Weissenbach J (1994) The 1993–94 Genethon human genetic linkage map. Nat Genet 7:246–249
4. Hayama K, Sugai N, Tanaka S, Lee S, Kikuchi H, Ito J, Suzuki J, Nagata Y, Kondo H, Harayama O, et al. (1989) High-incidence of C9 deficiency throughout Japan: there are no significant differences in incidence among eight areas of Japan. Int Arch Allergy Appl Immunol 90:400–404
5. Horiuchi T, Nishizaka H, Kojima T, Sawabe T, Niho Y, Schneider PM, Inaba S, Sakai K, Hayashi K, Hashimura C, Fukumori Y (1998) A non-sense mutation at Arg95 is predominant in complement 9 deficiency in Japanese. J Immunol 160:1509–1513
Cited by
19 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