https://www.selleckchem.com/pr....oducts/stat-in-1.htm
Familial cases of adult acute myeloid leukemia (AML) with germline-mutated CCAAT/enhancer-binding protein-α (CEBPA) gene are a rare entity classified in World Health Organization (WHO) classification 2016. Most families reported in the literature show an autosomal dominant inheritance pattern consistent with a single-gene mutation. Here we studied a Syrian family with four individuals suffering from AML for CEBPA gene mutations by Sanger sequencing. The father, his three affected, and one yet unaffected child had the same mutation in
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