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Genome-Wide Association Study of Copy Number Variations in Patients with Familial Neurocardiogenic Syncope.

Demir, Emre

Genome-Wide Association Study of Copy Number Variations in Patients with Familial Neurocardiogenic Syncope. [electronic resource] - Biochemical genetics Aug 2016 - 487-494 p. digital

Publication Type: Journal Article

ISSN: 1573-4927

Standard No.: 10.1007/s10528-016-9735-z doi

Subjects--Topical Terms:
Adolescent
Adult
DNA Copy Number Variations
Female
Genome-Wide Association Study--methods
Genotype
Humans
Male
Oligonucleotide Array Sequence Analysis
Syncope, Vasovagal--genetics
Young Adult

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