Factor XI deficiency: identification of six novel missense mutations (P23L, P69T, C92G, E243D, W497C and E547K).

MLA

Quélin, Florence, et al. “Factor XI Deficiency: Identification of Six Novel Missense Mutations (P23L, P69T, C92G, E243D, W497C and E547K).” Haematologica, vol. 90, no. 8, Aug. 2005, pp. 1149–50. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=cmedm&AN=16079124&authtype=sso&custid=ns315887.

APA

Quélin, F., François, D., d’Oiron, R., Guillet, B., de Raucourt, E., & de Mazancourt, P. (2005). Factor XI deficiency: identification of six novel missense mutations (P23L, P69T, C92G, E243D, W497C and E547K). Haematologica, 90(8), 1149–1150.

Chicago

Quélin, Florence, Dominique François, Roseline d’Oiron, Benoît Guillet, Emmanuelle de Raucourt, and Philippe de Mazancourt. 2005. “Factor XI Deficiency: Identification of Six Novel Missense Mutations (P23L, P69T, C92G, E243D, W497C and E547K).” Haematologica 90 (8): 1149–50. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=cmedm&AN=16079124&authtype=sso&custid=ns315887.