Levo A.,2000
Levo A., Kuismanen K., Holopainen P., Vahtera E., Rasi V., Krusius T., Partanen J. Single founder mutation (W-380-G) in type II protein C deficiency in Finland. - Thromb.Haemost., 2000, v. 84, p. 424-428.
Levo A., Kuismanen K., Holopainen P., Vahtera E., Rasi V., Krusius T., Partanen J. Single founder mutation (W-380-G) in type II protein C deficiency in Finland. - Thromb.Haemost., 2000, v. 84, p. 424-428.
