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89 Hypertens Res Vol.31 (2008) No.1 p.8996Original ArticleAssociation of CT Dinucleotide Repeat Polymorphism in the 5Flanking Region of the Guanylyl Cyclase (GC)A Gene with Essential Hypertension
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The association of CT dinucleotide refers to a genetic sequence involving the pairing of cytosine (C) and thymine (T) nucleotides. It is often studied in the context of genetic variations and their implications in health and disease.
Researchers and organizations conducting genetic studies or clinical trials may be required to file reports involving the association of CT dinucleotide, particularly when relevant to genetic risk assessment or public health.
Filling out the association of CT dinucleotide usually involves completing forms that detail the genetic data collected, analysis methods used, and findings related to the CT dinucleotide association, ensuring compliance with regulatory guidelines.
The purpose of the association of CT dinucleotide is to investigate its role in genetic variation, understand its impact on phenotypes, and assess its relevance in various diseases or health conditions.
Information that must be reported includes the specific genetic variants studied, sample demographics, methodologies, results, statistical analyses, and any conclusions drawn regarding the association of the CT dinucleotide with health outcomes.
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