Identification of a novel heterozygous <scp> <i>SOX9</i> </scp> variant in a Chinese family with congenital heart disease-Reference-Cited by-同舟云学术

Identification of a novel heterozygous SOX9 variant in a Chinese family with congenital heart disease

Published:2022-02-26 Issue:5 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Gong Li¹,Wang Chunyan²³,Xie Haiyang¹,Gao Jun⁴,Li Tengyan³,Qi Shenggui⁵,Wang Binbin²³^ORCID,Wang Jing⁶^ORCID

Affiliation:

1. Department of Cardiothoracic Surgery, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College Huazhong University of Science & Technology Wuhan China

2. Graduate School of Peking Union Medical College & Chinese Academy of Medical Sciences Beijing China

3. Center for Genetics National Research Institute for Family Planning Beijing China

4. Department of Ultrasound imaging, Wuhan Children's Hospital (Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College Huazhong University of Science & Technology Wuhan China

5. Qinghai High Altitude Medical Research Institute Xining China

6. Department of Medical Genetics and Developmental Biology, School of Basic Medical Sciences Capital Medical University Beijing China

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1909

Reference41 articles.

1. Congenital heart disease in 37,294 births in Tunisia: birth prevalence and mortality rate

2. Essential role of Sox9 in the pathway that controls formation of cardiac valves and septa

3. Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study

4. Congenital heart disease: current knowledge about causes and inheritance

5. Phylogeny of the SOX Family of Developmental Transcription Factors Based on Sequence and Structural Indicators

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