SOX17 loss-of-function variation underlying familial congenital heart disease-Reference-Cited by-同舟云学术

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SOX17 loss-of-function variation underlying familial congenital heart disease

Published:2021-05 Issue:5 Volume:64 Page:104211
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Zhao Lan,Jiang Wei-Feng,Yang Chen-Xi,Qiao Qi,Xu Ying-Jia,Shi Hong-Yu,Qiu Xing-Biao,Wu Shao-Hui,Yang Yi-Qing

Funder

Shanghai City Science and Technology Commission

Shanghai Medical College of Fudan University

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference92 articles.

1. Impaired pulmonary function and its association with clinical outcomes, exercise capacity and quality of life in children with congenital heart disease;Abassi;Int. J. Cardiol.,2019

2. The MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10;Agarwal;Development,2011

3. Cardiac transcription factor Csx/Nkx2-5: its role in cardiac development and diseases;Akazawa;Pharmacol. Ther.,2005

4. Identification of clinically actionable variants from genome sequencing of families with congenital heart disease;Alankarage;Genet. Med.,2019

5. Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease;Alankarage;Hum. Mol. Genet.,2020

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