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Systematic search for variation in the human norepinephrine transporter gene: identification of five naturally occurring missense mutations and study of association with major psychiatric disorders.
Stöber G, Nöthen MM, Pörzgen P, Brüss M, Bönisch H, Knapp M, Beckmann H, Propping P. Stöber G, et al. Among authors: bonisch h. Am J Med Genet. 1996 Nov 22;67(6):523-32. doi: 10.1002/(SICI)1096-8628(19961122)67:6<523::AID-AJMG3>3.0.CO;2-I. Am J Med Genet. 1996. PMID: 8950409
Association of major depression with rare functional variants in norepinephrine transporter and serotonin1A receptor genes.
Haenisch B, Linsel K, Brüss M, Gilsbach R, Propping P, Nöthen MM, Rietschel M, Fimmers R, Maier W, Zobel A, Höfels S, Guttenthaler V, Göthert M, Bönisch H. Haenisch B, et al. Among authors: bonisch h. Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):1013-6. doi: 10.1002/ajmg.b.30912. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 19105200
170 results