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
Me gusta
Comentario
Compartir
