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Hikmet Hakan Aydin on Muck Rack

Hikmet Hakan Aydin

As seen in: Biochemical Genetics
Former Dean, husband and father
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Genome-Wide Association Study of Copy Number Variations in Patients with Familial Neurocardiogenic Syncope

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By Emre Demir, Can Hasdemir, Handan Ak, Sevcan Atay, Hikmet Hakan Aydin
| Biochemical Genetics Verified
Neurocardiogenic syncope (NCS) is the most frequent type of syncope characterized by a self-limited episode of systemic hypotension. In this study, we conducted the first genome-wide association study testing copy number variations for association with NCS. Study population consisted of 107 consecutive patients with recurrent syncope and positive head-up tilt table testing. Four families with NCS were selected for CNV analysis. Affymetrix GeneChip® SNP 6.0 array was used for CNV analysis.
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