Single Nucleotide Variation Analysis in 65 Candidate Genes for CNS Disorders in a Representative Sample of the European Population

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 indic...

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Bibliografiska uppgifter
Huvudupphovsmän: Freudenberg-Hua, Yun, Freudenberg, Jan, Kluck, Nadine, Cichon, Sven, Propping, Peter, Nöthen, Markus M.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Cold Spring Harbor Laboratory Press 2003
Ämnen:
Letters
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC403700/
https://ncbi.nlm.nih.gov/pubmed/14525928
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.1299703
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