节段性单亲二体作为急性髓系白血病中纯合性CEBPA突变的反复出现机制。 - Suppr

Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia.

作者信息

Wouters B J, Sanders M A, Lugthart S, Geertsma-Kleinekoort W M C, van Drunen E, Beverloo H B, Löwenberg B, Valk P J M, Delwel R

出版信息

Leukemia. 2007 Nov;21(11):2382-4. doi: 10.1038/sj.leu.2404795. Epub 2007 Jun 7.

DOI:10.1038/sj.leu.2404795

PMID:17554374

Abstract

摘要

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Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia.

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