Conference Paper: Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations

TitleCrosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations
Authors
Issue Date2010
PublisherCanadian College of Medical Geneticists.
Citation
The 34th Annual Scientific Meeting of the Canadian College of Medical Geneticists (CCMG 2010), Halifax, NS., 21-23 October 2010. In Abstract Book, 2010, p. 1 How to Cite?
AbstractThe X-linked gene, JARID1C, encodes a H3K4 demethylase. Mutations in this gene cause intellectual disability (ID). We hypothesized that JARID1C mutations would dysregulate DNA methylation at specific genomic targets ...
DescriptionCCMG Oral Abstract Presentations – Commonwealth A: A01
Persistent Identifierhttp://hdl.handle.net/10722/129886

 

DC FieldValueLanguage
dc.contributor.authorChung, BHYen_US
dc.contributor.authorGrafodatskaya, D-
dc.contributor.authorButcher, DT-
dc.contributor.authorScherer, SW-
dc.contributor.authorAbidi, FE-
dc.contributor.authorSchwartz, CE-
dc.contributor.authorWeksberg, R-
dc.date.accessioned2010-12-23T08:43:50Z-
dc.date.available2010-12-23T08:43:50Z-
dc.date.issued2010en_US
dc.identifier.citationThe 34th Annual Scientific Meeting of the Canadian College of Medical Geneticists (CCMG 2010), Halifax, NS., 21-23 October 2010. In Abstract Book, 2010, p. 1en_US
dc.identifier.urihttp://hdl.handle.net/10722/129886-
dc.descriptionCCMG Oral Abstract Presentations – Commonwealth A: A01-
dc.description.abstractThe X-linked gene, JARID1C, encodes a H3K4 demethylase. Mutations in this gene cause intellectual disability (ID). We hypothesized that JARID1C mutations would dysregulate DNA methylation at specific genomic targets ...-
dc.languageengen_US
dc.publisherCanadian College of Medical Geneticists.-
dc.relation.ispartofAnnual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2010-
dc.titleCrosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutationsen_US
dc.typeConference_Paperen_US
dc.identifier.emailChung, BHY: bhychung@hku.hken_US
dc.description.naturepostprint-
dc.identifier.hkuros183278en_US
dc.identifier.spage1-
dc.identifier.epage1-
dc.publisher.placeCanada-
dc.description.otherThe 34th Annual Scientific Meeting of the Canadian College of Medical Geneticists (CCMG 2010), Halifax, NS., 21-23 October 2010. In Abstract Book of the 34th CCMG, 2010, p. 1-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats