1. Liu, Zequn, Jiang, Yanmin, Fang, Fu, Li, Dong-Zhi, Liao, Can. 2023. ASXL3 gene mutations inhibit cell proliferation and promote cell apoptosis in mouse cardiomyocytes by upregulating lncRNA NONMMUT063967.2. In Biochemistry and biophysics reports, 35, 101505. doi:10.1016/j.bbrep.2023.101505. https://pubmed.ncbi.nlm.nih.gov/37435360/
2. Zhang, R, He, X H, Lin, H Y, Yang, X H. . [Bainbridge-Ropers syndrome with ASXL3 gene variation in a child and literature review]. In Zhonghua er ke za zhi = Chinese journal of pediatrics, 56, 138-141. doi:10.3760/cma.j.issn.0578-1310.2018.02.013. https://pubmed.ncbi.nlm.nih.gov/29429203/
3. Fu, Fang, Li, Ru, Lei, Ting-Ying, Li, Dong-Zhi, Liao, Can. 2020. Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease. In Human genetics, 140, 333-348. doi:10.1007/s00439-020-02200-z. https://pubmed.ncbi.nlm.nih.gov/32696347/
4. Schirwani, Schaida, Albaba, Shadi, Carere, Deanna Alexis, Pierson, Tyler Mark, Balasubramanian, Meena. 2021. Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3. In American journal of medical genetics. Part A, 185, 3446-3458. doi:10.1002/ajmg.a.62465. https://pubmed.ncbi.nlm.nih.gov/34436830/
5. Woods, Emily, Holmes, Nicola, Albaba, Shadi, Evans, Iwan R, Balasubramanian, Meena. 2024. ASXL3-related disorder: Molecular phenotyping and comprehensive review providing insights into disease mechanism. In Clinical genetics, 105, 470-487. doi:10.1111/cge.14506. https://pubmed.ncbi.nlm.nih.gov/38420660/
6. Wu, Ke, Cong, Yan. 2021. Case report : a novel ASXL3 gene variant in a Sudanese boy. In BMC pediatrics, 21, 557. doi:10.1186/s12887-021-03038-8. https://pubmed.ncbi.nlm.nih.gov/34886823/
7. Laquerriere, Annie, Jaber, Dana, Abiusi, Emanuela, Gitiaux, Cyril, Melki, Judith. 2021. Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita. In Journal of medical genetics, 59, 559-567. doi:10.1136/jmedgenet-2020-107595. https://pubmed.ncbi.nlm.nih.gov/33820833/
8. Hurtado, Rodrigo, Guirales, Fabian, Tirado, Carlos A. . ASXL1 Gene in AML. In Journal of the Association of Genetic Technologists, 47, 60-68. doi:. https://pubmed.ncbi.nlm.nih.gov/34140438/
9. Katoh, Masuko, Katoh, Masaru. . Identification and characterization of ASXL3 gene in silico. In International journal of oncology, 24, 1617-22. doi:. https://pubmed.ncbi.nlm.nih.gov/15138607/