(Q73128629)

English

A novel type of mutation at the propeptide cleavage site (AlA+1Thr) causing symptomatic protein C type II deficiency

scientific article published on 01 October 2000

Statements

A novel type of mutation at the propeptide cleavage site (AlA+1Thr) causing symptomatic protein C type II deficiency (English)

Identifiers

 
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