Single founder mutation (W380G) in type II protein C deficiency in Finland.

Added 5701 days ago (21.12.2005)
Authors: Levo A, Kuismanen K, Holopainen P, Vahtera E, Rasi V, Holopainen P, Rasi V, Krusius T, Partanen J
PubMed id: 11019966
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