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Article

Frequency of genetic mutations associated with thromboembolism in the Western Black Sea Region.

Internal medicine (Tokyo, Japan) - 1 Jan 2011

Tug Esra, Aydin Hatip, Kaplan Ebru, Dogruer Dilek

Abstract excerpt

OBJECTIVE: We aimed to determine the prevalences of important genetic causes of thromboembolism for the first time in the western Black Sea Region of Turkey. PATIENTS AND METHODS: One hundred and eighty-eight patients diagnosed early with thrombophilia were included in the study. The samples were genotyped using real-time LightCycler. RESULTS: Of the 188 patients, 179 (95.2%) had one or more mutations. The...

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PMID: 21212568
DOI: 10.2169/internalmedicine.50.4144

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MTHFR

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