Redefining the MED13L syndrome-Reference-Cited by-同舟云学术

Redefining the MED13L syndrome

Published:2015-03-11 Issue:10 Volume:23 Page:1308-1317
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Adegbola Abidemi,Musante Luciana,Callewaert Bert,Maciel Patricia,Hu Hao,Isidor Bertrand,Picker-Minh Sylvie,Le Caignec Cedric,Delle Chiaie Barbara,Vanakker Olivier,Menten Björn,Dheedene Annelies,Bockaert Nele,Roelens Filip,Decaestecker Karin,Silva João,Soares Gabriela,Lopes Fátima,Najmabadi Hossein,Kahrizi Kimia,Cox Gerald F,Angus Steven P,Staropoli John F,Fischer Ute,Suckow Vanessa,Bartsch Oliver,Chess Andrew,Ropers Hans-Hilger,Wienker Thomas F,Hübner Christoph,Kaindl Angela M,Kalscheuer Vera M

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg201526.pdf

Reference33 articles.

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4. Asadollahi R, Oneda B, Sheth F et al: Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability. Eur J Hum Genet 2013; 21: 1100–1104.

5. Davis MA, Larimore EA, Fissel BM, Swanger J, Taatjes DJ, Clurman BE : The SCF-Fbw7 ubiquitin ligase degrades MED13 and MED13L and regulates CDK8 module association with mediator. Genes Dev 2013; 27: 151–156.

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