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  Screening for rare variants in TMEM132D: a candidate gene from genome-wide association studies in anxiety disorders

Quast, C., Altmann, A., Weber, P., Rex-Haffner, M., Erhardt, A., Müller-Myhsok, B., et al. (2011). Screening for rare variants in TMEM132D: a candidate gene from genome-wide association studies in anxiety disorders. European Neuropsychopharmacology, 21(Suppl. 1), S6-S7.

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Genre: Journal Article
Alternative Title : Eur. Neuropsychopharmacol.

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 Creators:
Quast, C.1, Author           
Altmann, A.2, Author           
Weber, P.3, Author           
Rex-Haffner, M.1, Author           
Erhardt, A.1, Author           
Müller-Myhsok, B.2, Author           
Binder, E. B.1, Author           
Affiliations:
1AG Binder, Elisabeth, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607142              
2AG Müller-Myhsok, Bertram, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607154              
3AG Deussing, Jan, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607145              

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Language(s): eng - English
 Dates: 2011-03
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 563260
ISI: 000289387200008
 Degree: -

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Title: European Neuropsychopharmacology
  Alternative Title : Eur. Neuropsychopharmacol.
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: AMSTERDAM : ELSEVIER SCIENCE BV
Pages: - Volume / Issue: 21 (Suppl. 1) Sequence Number: - Start / End Page: S6 - S7 Identifier: ISSN: 0924-977X