A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction.

Authors :: Wypasek E
Pankiw-Bembenek O
Potaczek DP
Alhenc-Gelas M
Trebacz J
Undas A
Source :: International journal of cardiology [Int J Cardiol] 2013 Sep 01; Vol. 167 (5), pp. e146-8. Date of Electronic Publication: 2013 May 03.
Publication Year :: 2013

Subjects :: Adult
Humans
Male
Myocardial Infarction complications
Myocardial Infarction diagnostic imaging
Protein C Deficiency complications
Protein C Deficiency diagnostic imaging
Radiography
Mutation, Missense genetics
Myocardial Infarction genetics
Protein C genetics
Protein C Deficiency genetics

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