Molecular characterisation of 36 multilocus imprinting disturbance (MLID) patients: a comprehensive approach

BACKGROUND: Imprinting disorders (ImpDis) comprise diseases which are caused by aberrant regulation of monoallelically and parent-of-origin-dependent expressed genes. A characteristic molecular change in ImpDis patients is aberrant methylation signatures at disease-specific loci, without an obvious...

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Detalles Bibliográficos
Autores principales: Bilo, Larissa, Ochoa, Eguzkine, Lee, Sunwoo, Dey, Daniela, Kurth, Ingo, Kraft, Florian, Rodger, Fay, Docquier, France, Toribio, Ana, Bottolo, Leonardo, Binder, Gerhard, Fekete, György, Elbracht, Miriam, Maher, Eamonn R., Begemann, Matthias, Eggermann, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979536/
https://www.ncbi.nlm.nih.gov/pubmed/36859312
http://dx.doi.org/10.1186/s13148-023-01453-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9979536/
https://www.ncbi.nlm.nih.gov/pubmed/36859312
http://dx.doi.org/10.1186/s13148-023-01453-5

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