Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
-
Englisch
- Erschienen in
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In: Molecular Psychiatry (2014) 19, 115–121; doi:10.1038/mp.2012.161
- Schlagwort
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Kinderheilkunde
Kinderkrankheit
- Ereignis
-
Veröffentlichung
- (wo)
-
Würzburg
- (wer)
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Universität Würzburg
- (wann)
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2015
- Urheber
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Jarick, I.
Volckmar, A. L.
Pütter, C.
Pechlivanis, S.
Nguyen, T. T.
Dauvermann, M. R.
Beck, S.
Albayrak, Ö.
Scherag, S.
Gilsbach, S.
Cichon, S.
Hoffmann, P.
Degenhardt, F.
Nöthen, M. M.
Schreiber, S.
Wichmann, H. E.
Jöckel, K. H.
Heinrich, J.
Tiesler, C. M. T.
Faraone, S. V.
Walitza, S.
Sinzig, J.
Freitag, C.
Meyer, J.
Herpertz-Dahlmann, Beate
Lehmkuhl, G.
Renner, T. J.
Warnke, A.
Romanos, M.
Lesch, K. P.
Reif, A.
Schimmelmann, B. G.
Hebebrand, J.
Scherag, A.
Hinney, A.
- URN
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urn:nbn:de:bvb:20-opus-121131
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:48 MEZ
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Beteiligte
- Jarick, I.
- Volckmar, A. L.
- Pütter, C.
- Pechlivanis, S.
- Nguyen, T. T.
- Dauvermann, M. R.
- Beck, S.
- Albayrak, Ö.
- Scherag, S.
- Gilsbach, S.
- Cichon, S.
- Hoffmann, P.
- Degenhardt, F.
- Nöthen, M. M.
- Schreiber, S.
- Wichmann, H. E.
- Jöckel, K. H.
- Heinrich, J.
- Tiesler, C. M. T.
- Faraone, S. V.
- Walitza, S.
- Sinzig, J.
- Freitag, C.
- Meyer, J.
- Herpertz-Dahlmann, Beate
- Lehmkuhl, G.
- Renner, T. J.
- Warnke, A.
- Romanos, M.
- Lesch, K. P.
- Reif, A.
- Schimmelmann, B. G.
- Hebebrand, J.
- Scherag, A.
- Hinney, A.
- Universität Würzburg
Entstanden
- 2015
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