Trans-acting genetic variants causing multilocus imprinting disturbance (MLID): common mechanisms and consequences

Imprinting disorders are a group of congenital diseases which are characterized by molecular alterations affecting differentially methylated regions (DMRs). To date, at least twelve imprinting disorders have been defined with overlapping but variable clinical features including growth and metabolic...

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Veröffentlicht in:	Clinical epigenetics 2022-03, Vol.14 (1), p.41, Article 41
Hauptverfasser:	Eggermann, Thomas, Yapici, Elzem, Bliek, Jet, Pereda, Arrate, Begemann, Matthias, Russo, Silvia, Tannorella, Pierpaola, Calzari, Luciano, de Nanclares, Guiomar Perez, Lombardi, Paola, Temple, I Karen, Mackay, Deborah, Riccio, Andrea, Kagami, Masayo, Ogata, Tsutomu, Lapunzina, Pablo, Monk, David, Maher, Eamonn R, Tümer, Zeynep
Format:	Artikel
Sprache:	eng
Schlagworte:	Adaptor Proteins, Signal Transducing - genetics Beckwith-Wiedemann Syndrome - genetics Book publishing CCAAT-Enhancer-Binding Proteins - genetics Diabetes DNA Methylation Female Genetic disorders Genetic research Genomic Imprinting Humans Maternal Inheritance Medical colleges Methylation Pregnancy Silver-Russell Syndrome - diagnosis Silver-Russell Syndrome - genetics Ubiquitin-Protein Ligases - genetics
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