Erratum: Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms

Correction to: Molecular Psychiatry advance online publication, 19 July 2016; doi:10.1038/mp.2016.101 In the abstract, the P-value of the white matter lesions should have been listed as 3.3 × 10−02. Also in the abstract, the higher risk of Alzheimer’s disease should have been listed as an odds ratio...

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Published inMolecular psychiatry Vol. 22; no. 4; p. 634
Main Authors Amin, N, Jovanova, O, Adams, H H H, Dehghan, A, Kavousi, M, Vernooij, M W, Peeters, R P, de Vrij, F M S, van der Lee, S J, van Rooij, J G J, van Leeuwen, E M, Chaker, L, Demirkan, A, Hofman, A, Brouwer, R W W, Kraaij, R, Willems van Dijk, K, Hankemeier, T, van Ijcken, W F J, Uitterlinden, A G, Niessen, W J, Franco, O H, Kushner, S A, Ikram, M A, Tiemeier, H, van Duijn, C M
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.04.2017
Nature Publishing Group
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Online AccessGet full text
ISSN1359-4184
1476-5578
DOI10.1038/mp.2016.141

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Summary:Correction to: Molecular Psychiatry advance online publication, 19 July 2016; doi:10.1038/mp.2016.101 In the abstract, the P-value of the white matter lesions should have been listed as 3.3 × 10−02. Also in the abstract, the higher risk of Alzheimer’s disease should have been listed as an odds ratio, not an odds ration.
Bibliography:erratum
ObjectType-Correction/Retraction-1
SourceType-Scholarly Journals-1
content type line 14
ISSN:1359-4184
1476-5578
DOI:10.1038/mp.2016.141