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STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability


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16 citations in Scopus®
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Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > Institute of Medical Genetics
Dewey Decimal Classification:570 Life sciences; biology
610 Medicine & health
Scopus Subject Areas:Life Sciences > Genetics
Health Sciences > Genetics (clinical)
Uncontrolled Keywords:Cohesin, Intellectual disability, STAG1, datasharing
Language:English
Date:July 2017
Deposited On:13 Nov 2017 15:36
Last Modified:28 Jul 2020 11:48
Publisher:BMJ Publishing Group
ISSN:0022-2593
OA Status:Closed
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:https://doi.org/10.1136/jmedgenet-2016-104468
PubMed ID:28119487

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