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Article

Single nucleotide variation analysis in 65 candidate genes for CNS disorders in a representative sample of the European population.

Genome research - 1 Oct 2003

Freudenberg-Hua Yun, Freudenberg Jan, Kluck Nadine, Cichon Sven, Propping Peter, Nöthen Markus M

Abstract excerpt

The detailed investigation of variation in functionally important regions of the human genome is expected to promote understanding of genetically complex diseases. We resequenced 65 candidate genes for CNS disorders in an average of 85 European individuals. The minor allele frequency (MAF), an in...

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PMID: 14525928
DOI: 10.1101/gr.1299703
PMCID: PMC403700

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MAF

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-14525928-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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