Identification and pathogenicity of a novel c.509-2A>G variant in the causative gene RUNX1 for familial platelet disorder with a predisposition to acute myeloid leukemia

MA Jingjing, ZHANG Chengcheng, DENG Mei, LIN Weixia, GUO Li, SONG Yuanzong

Journal of Jinan University Natural Science & Medicine Edition ›› 2025, Vol. 46 ›› Issue (3) : 366-374.

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Journal of Jinan University Natural Science & Medicine Edition ›› 2025, Vol. 46 ›› Issue (3) : 366-374. DOI: 10.11778/j.jdxb.20250005
Research on clinical medicine

Identification and pathogenicity of a novel c.509-2A>G variant in the causative gene RUNX1 for familial platelet disorder with a predisposition to acute myeloid leukemia

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{{article.zuoZheEn_L}}. {{article.title_en}}. {{journal.qiKanMingCheng_EN}}. 2025, 46(3): 366-374 https://doi.org/10.11778/j.jdxb.20250005

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