Correction: Functional significance of rare neuroligin 1 variants found in autism.

Correction: Functional significance of rare neuroligin 1 variants found in autism.

[This corrects the article DOI: 10.1371/journal.pgen.1006940.].

Bibliographic Details
Main Authors: Moe Nakanishi, Jun Nomura, Xiao Ji, Kota Tamada, Takashi Arai, Eiki Takahashi, Maja Bućan, Toru Takumi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-10-01
Series:PLoS Genetics
Online Access:http://europepmc.org/articles/PMC5626024?pdf=render
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spelling doaj-beb153ad20ce48a98103afadcff117fc2020-11-25T02:30:15ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042017-10-011310e100703510.1371/journal.pgen.1007035Correction: Functional significance of rare neuroligin 1 variants found in autism.Moe NakanishiJun NomuraXiao JiKota TamadaTakashi AraiEiki TakahashiMaja BućanToru Takumi[This corrects the article DOI: 10.1371/journal.pgen.1006940.].http://europepmc.org/articles/PMC5626024?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Moe Nakanishi
Jun Nomura
Xiao Ji
Kota Tamada
Takashi Arai
Eiki Takahashi
Maja Bućan
Toru Takumi
spellingShingle Moe Nakanishi
Jun Nomura
Xiao Ji
Kota Tamada
Takashi Arai
Eiki Takahashi
Maja Bućan
Toru Takumi
Correction: Functional significance of rare neuroligin 1 variants found in autism.
PLoS Genetics
author_facet Moe Nakanishi
Jun Nomura
Xiao Ji
Kota Tamada
Takashi Arai
Eiki Takahashi
Maja Bućan
Toru Takumi
author_sort Moe Nakanishi
title Correction: Functional significance of rare neuroligin 1 variants found in autism.
title_short Correction: Functional significance of rare neuroligin 1 variants found in autism.
title_full Correction: Functional significance of rare neuroligin 1 variants found in autism.
title_fullStr Correction: Functional significance of rare neuroligin 1 variants found in autism.
title_full_unstemmed Correction: Functional significance of rare neuroligin 1 variants found in autism.
title_sort correction: functional significance of rare neuroligin 1 variants found in autism.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2017-10-01
description [This corrects the article DOI: 10.1371/journal.pgen.1006940.].
url http://europepmc.org/articles/PMC5626024?pdf=render
work_keys_str_mv AT moenakanishi correctionfunctionalsignificanceofrareneuroligin1variantsfoundinautism
AT junnomura correctionfunctionalsignificanceofrareneuroligin1variantsfoundinautism
AT xiaoji correctionfunctionalsignificanceofrareneuroligin1variantsfoundinautism
AT kotatamada correctionfunctionalsignificanceofrareneuroligin1variantsfoundinautism
AT takashiarai correctionfunctionalsignificanceofrareneuroligin1variantsfoundinautism
AT eikitakahashi correctionfunctionalsignificanceofrareneuroligin1variantsfoundinautism
AT majabucan correctionfunctionalsignificanceofrareneuroligin1variantsfoundinautism
AT torutakumi correctionfunctionalsignificanceofrareneuroligin1variantsfoundinautism
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