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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Detalles Bibliográficos
Publicado en:Clin Epigenetics
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2015
Assuntos:
Review
Acceso en liña: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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