Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences
Author:
Funder
Inserm
Université Paris Descartes
Association Française du Syndrome de Rett
Labex “Who I am?”
Publisher
Elsevier BV
Subject
Genetics,General Medicine
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3. Next generation sequencing in nonsyndromic intellectual disability: from a negative molecular karyotype to a possible causative mutation detection;Athanasakis;Am. J. Med. Genet. A,2014
4. SUMOylation negatively modulates target gene occupancy of the KDM5B, a histone lysine demethylase;Bueno;Epigenetics,2013
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