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J.1365-2141.1995.TB05214.X
J.1365-2141.1995.TB05214.X
http://dx.doi.org/10.1111/J.1365-2141.1995.TB05214.X
Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain.
P356
Q34304894-3DC730B4-188C-44E8-B184-DEF87CF519EF
P356
J.1365-2141.1995.TB05214.X
http://dx.doi.org/10.1111/J.1365-2141.1995.TB05214.X