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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Coronary artery disease and ABCC6[original query]
Frequent mutation in the ABCC6 gene (R1141X) is associated with a strong increase in the prevalence of coronary artery disease.
Circulation 2002 Aug 106 (7): 773-5.
Trip Mieke D, Smulders Yvo M, Wegman Jurgen J, Hu Xiaofeng, Boer Jolanda M A, ten Brink Jacoline B, Zwinderman Aeilko H, Kastelein John J P, Feskens Edith J M, Bergen Arthur A
Assessment of a rapid-cycle PCR assay for the identification of the recurrent c.3421C>T mutation in the ABCC6 gene in pseudoxanthoma elasticum patients.
Laboratory investigation; a journal of technical methods and pathology 2004 Jan 84 (1): 122-30.
Götting Christian, Schulz Veronika, Hendig Doris, Grundt Alexander, Dreier Jens, Szliska Christiane, Brinkmann Thomas, Kleesiek Kn
The R1141X loss-of-function mutation of the ABCC6 gene is a strong genetic risk factor for coronary artery disease.
Genetic testing and molecular biomarkers 2010 Feb 14 (1): 75-8.
Köblös Gabriella, Andrikovics Hajnalka, Prohászka Zoltán, Tordai Attila, Váradi András, Arányi Tam
Genetic variants in cardiac calcification in Northern Sweden.
Medicine 2019 4 98 (15): e15065.
Hellman Urban, Mörner Stellan, Henein Micha
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