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Deletion of parental GST genes as a possible susceptibility factor in the etiology of infant leukemia.

作者信息

Garte S, Taioli E, Crosti F, Sainati L, Barisone E, Luciani M, Jankovic M, Biondi A G

机构信息

UMDNJ-Robert Wood Johnson Medical School, Piscataway, NJ 08854, USA.

出版信息

Leuk Res. 2000 Nov;24(11):971-4. doi: 10.1016/s0145-2126(00)00052-7.

DOI:10.1016/s0145-2126(00)00052-7
PMID:11086181
Abstract

Infant leukemia below the age of 12 months is a rare disease that exhibits a high frequency of 11q23 rearrangements. We assessed the presence of polymorphisms in several metabolic genes in 23 families of infants diagnosed with leukemia under 12 months of age in Italy. When polymorphism frequencies were calculated within families, frequencies of GST gene deletions were significantly higher than expected only among the parents of infants without the 11q23 rearrangement. These data suggest that the deletion of GST genes in parents may affect the risk of infant leukemia through a pathway independent of the MLL gene.

摘要

相似文献

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