Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease-Reference-Cited by-同舟云学术

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Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease

Published:2020-07-21 Issue:2 Volume:140 Page:333-348
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Fu Fang,Li Ru,Lei Ting-ying,Wang Dan,Yang Xin,Han Jin,Pan Min,Zhen Li,Li Jian,Li Fa-tao,Jing Xiang-yi,Li Dong-zhi,Liao Can^ORCID

Funder

National Natural Science Foundation of China

Natural Science Foundation of Guangdong Province

Major Project of the Department of Science and Technology of Guangdong Province

Major Project of the Department of Science and Technology of Guangzhou

Municipal Healthcare Joint-Innovation Major Project of Guangzhou phase III

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

https://link.springer.com/content/pdf/10.1007/s00439-020-02200-z.pdf

Reference26 articles.

1. Abdel-Wahab O, Gao J, Adli M et al (2013) Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo. J Exp Med 210:2641–2659. https://doi.org/10.1084/jem.20131141

2. Bruneau BG (2008) The developmental genetics of congenital heart disease. Nature 451:943–948. https://doi.org/10.1038/nature06801

3. Bruneau BG (2013) Signaling and transcriptional networks in heart development and regeneration. Cold Spring Harbor Perspect Biol 5:a008292. https://doi.org/10.1101/cshperspect.a008292

4. Delgado-Olguin P, Huang Y, Li X et al (2012) Epigenetic repression of cardiac progenitor gene expression by Ezh2 is required for postnatal cardiac homeostasis. Nat Genet 44:343–347. https://doi.org/10.1038/ng.1068

5. Duployez N, Micol JB, Boissel N et al (2016) Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21). Leukemia Lymphoma 57:199–200. https://doi.org/10.3109/10428194.2015.1037754

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