Transcriptional profiling at the DLK1/MEG3 domain explains clinical overlap between imprinting disorders

Imprinting disorders (IDs) often affect growth in humans, leading to diseases with overlapping features, regardless of the genomic region affected. IDs related to hypomethylation of the human 14q32.2 region and its DLK1/MEG3 domain are associated with Temple syndrome (TS14). TS14 is a rare type of g...

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Detalles Bibliográficos
Autores principales: Abi Habib, Walid, Brioude, Frédéric, Azzi, Salah, Rossignol, Sylvie, Linglart, Agnès, Sobrier, Marie-Laure, Giabicani, Éloïse, Steunou, Virginie, Harbison, Madeleine D., Le Bouc, Yves, Netchine, Irène
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382400/
https://www.ncbi.nlm.nih.gov/pubmed/30801013
http://dx.doi.org/10.1126/sciadv.aau9425

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6382400/
https://www.ncbi.nlm.nih.gov/pubmed/30801013
http://dx.doi.org/10.1126/sciadv.aau9425

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