Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations

Research output: Contribution to journal › Article › peer-review

CESD, Depressive symptoms, Exome sequencing, Major depression, MDD, NKPD1, European Continental Ancestry Group/genetics, Genome-Wide Association Study, Humans, Middle Aged, Membrane Proteins/genetics, Male, Nucleoside-Triphosphatase/genetics, Depressive Disorder, Major/genetics, Exome, Genetic Variation, Depression/genetics, Netherlands, Nerve Tissue Proteins/genetics, Female, Polymorphism, Single Nucleotide, METAANALYSIS, RARE, CELL-LINES, INDIVIDUALS, SERINE PALMITOYLTRANSFERASE, GENOME-WIDE ASSOCIATION, VARIANTS, MAJOR DEPRESSION, LESCH-NYHAN-DISEASE, SEQUENCING DATA

ID: 10041002