A 2q24.2 microdeletion containingTANKas novel candidate gene for intellectual disability
Author:
Affiliation:
1. Department of Dermatology; University Hospital Magdeburg, University of Magdeburg; Magdeburg Germany
2. Institute of Human Genetics; Otto-von-Guericke University; Magdeburg Germany
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.61093/fullpdf
Reference22 articles.
1. Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex;Bedogni;Proceedings of the National Academy of Sciences of the United States of America,2010
2. A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14;Burrage;American Journal of Medical Genetics: Part A,2013
3. The UCSC genome browser database. 2018 update;Casper;Nucleic Acids Research,2018
4. Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-q24.3 in a girl with autistic features and developmental delay;Chen;European Journal of Medical Genetics,2010
5. TANK, a co-inducer with TRAF2 of TNF- and CD 40L-mediated NF-kappaB activation;Cheng;Genes & Development,1996
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3. De novo TBR1 variants cause a neurocognitive phenotype with ID and autistic traits: report of 25 new individuals and review of the literature;European Journal of Human Genetics;2020-01-31
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