Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding

Epistatic interaction of genetic depression risk variants in the human subgenual cingulate cortex during memory encoding

Recent genome-wide association studies have pointed to single-nucleotide polymorphisms (SNPs) in genes encoding the neuronal calcium channel CaV1.2 (CACNA1C; rs1006737) and the presynaptic active zone protein Piccolo (PCLO; rs2522833) as risk factors for affective disorders, particularly major depre...

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Main Authors: Schott, B H, Assmann, A, Schmierer, P, Soch, J, Erk, S, Garbusow, M, Mohnke, S, Pöhland, L, Romanczuk-Seiferth, N, Barman, A, Wüstenberg, T, Haddad, L, Grimm, O, Witt, S, Richter, S, Klein, M, Schütze, H, Mühleisen, T W, Cichon, S, Rietschel, M, Noethen, M M, Tost, H, Gundelfinger, E D, Düzel, E, Heinz, A, Meyer-Lindenberg, A, Seidenbecher, C I, Walter, H
Format: Online
Language:English
Published: Nature Publishing Group 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966038/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3966038/

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