A novel de novo frameshift deletion in EHMT1 in a patient with Kleefstra Syndrome results in decreased H3K9 dimethylation

BACKGROUND: Kleefstra Syndrome (KS) (MIM# 610253) is an autosomal dominant disorder caused by haploinsufficiency of euchromatic histone methyltransferase‐1 (EHMT1, GLP). EHMT1 (MIM# 607001) encodes a histone methyltransferase that heterodimerizes with EHMT2 (also known as G9a, MIM# 604599), which to...

Descripción completa

Detalles Bibliográficos
Autores principales: Blackburn, Patrick R., Williams, Monique, Cousin, Margot A., Boczek, Nicole J., Beek, Geoffrey J., Lomberk, Gwen A., Urrutia, Raul A., Babovic‐Vuksanovic, Dusica, Klee, Eric W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Clinical Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370226/
https://www.ncbi.nlm.nih.gov/pubmed/28361100
http://dx.doi.org/10.1002/mgg3.268

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5370226/
https://www.ncbi.nlm.nih.gov/pubmed/28361100
http://dx.doi.org/10.1002/mgg3.268

Ejemplares similares