3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances
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| Format: | Online |
| Language: | English |
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BioMed Central
2015
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628252/ |
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pubmed-4628252 |
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pubmed-46282522015-11-01 3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances Iourov, Ivan Y. Vorsanova, Svetlana G. Voinova, Victoria Y. Yurov, Yuri B. Research BioMed Central 2015-10-31 /pmc/articles/PMC4628252/ /pubmed/26523151 http://dx.doi.org/10.1186/s13039-015-0185-9 Text en © Iourov et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
| repository_type |
Open Access Journal |
| institution_category |
Foreign Institution |
| institution |
US National Center for Biotechnology Information |
| building |
NCBI PubMed |
| collection |
Online Access |
| language |
English |
| format |
Online |
| author |
Iourov, Ivan Y. Vorsanova, Svetlana G. Voinova, Victoria Y. Yurov, Yuri B. |
| spellingShingle |
Iourov, Ivan Y. Vorsanova, Svetlana G. Voinova, Victoria Y. Yurov, Yuri B. 3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances |
| author_facet |
Iourov, Ivan Y. Vorsanova, Svetlana G. Voinova, Victoria Y. Yurov, Yuri B. |
| author_sort |
Iourov, Ivan Y. |
| title |
3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances |
| title_short |
3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances |
| title_full |
3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances |
| title_fullStr |
3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances |
| title_full_unstemmed |
3p22.1p21.31 microdeletion identifies CCK as Asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances |
| title_sort |
3p22.1p21.31 microdeletion identifies cck as asperger syndrome candidate gene and shows the way for therapeutic strategies in chromosome imbalances |
| description |
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| publisher |
BioMed Central |
| publishDate |
2015 |
| url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4628252/ |
| _version_ |
1613495685079891968 |