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Literature DB >> 23643436

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

Ewa Wypasek, Oksana Pankiw-Bembenek, Daniel P Potaczek, Martine Alhenc-Gelas, Jaroslaw Trebacz, Anetta Undas.

Abstract

Entities: Disease Mutation Species

Keywords: Mutation; PROC; Protein C deficiency; STEMI

Mesh：

Substances：
Protein C

Year: 2013 PMID： 23643436 DOI： 10.1016/j.ijcard.2013.04.102

Source DB: PubMed Journal: Int J Cardiol ISSN： 0167-5273 Impact factor: 4.164

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1 in total

1. A Series of 14 Polish Patients with Thrombotic Events and PC Deficiency-Novel c.401-1G>A PROC Gene Splice Site Mutation in a Patient with Aneurysms.

Authors: Anna Weronska; Daniel P Potaczek; Julia Oto; Pilar Medina; Anetta Undas; Ewa Wypasek
Journal: Genes (Basel) Date: 2022-04-22 Impact factor: 4.141

1 in total

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

1. A Series of 14 Polish Patients with Thrombotic Events and PC Deficiency-Novel c.401-1G&gt;A PROC Gene Splice Site Mutation in a Patient with Aneurysms.

1. A Series of 14 Polish Patients with Thrombotic Events and PC Deficiency-Novel c.401-1G>A PROC Gene Splice Site Mutation in a Patient with Aneurysms.