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RUNX1T1, a chromatin repression protein, is a candidate gene for autosomal dominant intellectual disability

✍ Scribed by Minh Tuan Huynh; Mylène Béri-Dexheimer; Céline Bonnet; Myriam Bronner; Asma Ali Khan; Lila Allou; Christophe Philippe; Jacqueline Vigneron; Philippe Jonveaux

Book ID
111995211
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
402 KB
Volume
158A
Category
Article
ISSN
1552-4825

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## Abstract A partial deletion of chromosome band 2p25.3 (2pter) is a rarely described cytogenetic aberration in patients with intellectual disability (ID). Using microarrays we identified deletions of 2p25.3, sized 0.37–3.13 Mb, in three adult siblings and three unrelated patients. All patients ha