MOZ Regulates the Tbx1 Locus, and Moz Mutation Partially Phenocopies DiGeorge Syndrome

DiGeorge syndrome, caused by a 22q11 microdeletion or mutation of the TBX1 gene, varies in severity greatly, even among monozygotic twins. Epigenetic phenomena have been invoked to explain phenotypic differences in individuals of identical genetic composition, although specific chromatin modificatio...

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Auteurs principaux: Voss, Anne K., Vanyai, Hannah K., Collin, Caitlin, Dixon, Mathew P., McLennan, Tamara J., Sheikh, Bilal N., Scambler, Peter, Thomas, Tim
Format: Artigo
Langue:Inglês
Publié: Cell Press 2012
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3442180/
https://ncbi.nlm.nih.gov/pubmed/22921202
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.devcel.2012.07.010
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