RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome-Reference-Cited by-同舟云学术

RAP1-mediated MEK/ERK pathway defects in Kabuki syndrome

Published:2015-08-17 Issue:9 Volume:125 Page:3585-3599
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Bögershausen Nina,Tsai I-Chun,Pohl Esther,Kiper Pelin Özlem Simsek,Beleggia Filippo,Percin E. Ferda,Keupp Katharina,Matchan Angela,Milz Esther,Alanay Yasemin,Kayserili Hülya,Liu Yicheng,Banka Siddharth,Kranz Andrea,Zenker Martin,Wieczorek Dagmar,Elcioglu Nursel,Prontera Paolo,Lyonnet Stanislas,Meitinger Thomas,Stewart A. Francis,Donnai Dian,Strom Tim M.,Boduroglu Koray,Yigit Gökhan,Li Yun,Katsanis Nicholas,Wollnik Bernd

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference50 articles.

1. Skirting the pitfalls: a clear‐cut nomenclature for H3K4 methyltransferases

2. Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome

3. Deletion of KDM6A, a Histone Demethylase Interacting with MLL2, in Three Patients with Kabuki Syndrome

4. KDM6A Point Mutations Cause Kabuki Syndrome

5. Unmasking Kabuki syndrome

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