Imprinting disorders: a group of congenital disorders with overlapping patterns of molecular changes affecting imprinted loci

Congenital imprinting disorders (IDs) are characterised by molecular changes affecting imprinted chromosomal regions and genes, i.e. genes that are expressed in a parent-of-origin specific manner. Recent years have seen a great expansion in the range of alterations in regulation, dosage or DNA seque...

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Détails bibliographiques
Publié dans:Clin Epigenetics
Auteurs principaux: Eggermann, Thomas, Perez de Nanclares, Guiomar, Maher, Eamonn R., Temple, I. Karen, Tümer, Zeynep, Monk, David, Mackay, Deborah J. G., Grønskov, Karen, Riccio, Andrea, Linglart, Agnès, Netchine, Irène
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2015
Sujets:
Review
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4650860/
https://ncbi.nlm.nih.gov/pubmed/26583054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13148-015-0143-8
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