1. Sportoletti, Paolo, Sorcini, Daniele, Falini, Brunangelo. . BCOR gene alterations in hematologic diseases. In Blood, 138, 2455-2468. doi:10.1182/blood.2021010958. https://pubmed.ncbi.nlm.nih.gov/33945606/
2. Li, Meng, Collins, Roxane, Jiao, Yuchen, Papadopoulos, Nickolas, Malek, Sami N. 2011. Somatic mutations in the transcriptional corepressor gene BCORL1 in adult acute myelogenous leukemia. In Blood, 118, 5914-7. doi:10.1182/blood-2011-05-356204. https://pubmed.ncbi.nlm.nih.gov/21989985/
3. Cen, Yan-Xia, Li, Yan. . [Clinical Characteristics and Prognostic Significance of BCOR/BCORL1 Gene Mutation in Patients with Myelodysplastic Syndromes]. In Zhongguo shi yan xue ye xue za zhi, 28, 2004-2010. doi:10.19746/j.cnki.issn.1009-2137.2020.06.034. https://pubmed.ncbi.nlm.nih.gov/33283733/
4. Yoshizato, Tetsuichi, Dumitriu, Bogdan, Hosokawa, Kohei, Young, Neal S, Ogawa, Seishi. . Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia. In The New England journal of medicine, 373, 35-47. doi:10.1056/NEJMoa1414799. https://pubmed.ncbi.nlm.nih.gov/26132940/
5. Luo, Chen, Chen, Zixu, Meng, Lanlan, Tan, Yue-Qiu, Hu, Tong-Yao. 2024. A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia. In Clinical genetics, 106, 27-36. doi:10.1111/cge.14500. https://pubmed.ncbi.nlm.nih.gov/38342987/
6. Muthusamy, Babylakshmi, Bellad, Anikha, Girimaji, Satish Chandra, Pandey, Akhilesh. 2021. Shukla-Vernon Syndrome: A Second Family with a Novel Variant in the BCORL1 Gene. In Genes, 12, . doi:10.3390/genes12030452. https://pubmed.ncbi.nlm.nih.gov/33810051/
7. Wang, Yu, Xiang, Mingfei, Zhou, Yiru, Cao, Yunxia, Zhu, Fuxi. 2024. Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription. In Andrology, , . doi:10.1111/andr.13743. https://pubmed.ncbi.nlm.nih.gov/39189935/
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