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资源简介：
22Rv1_FOXA1_Dex_rep1
应用场景：
创建时间：
2023-03-09
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Novel human cellular model of CDA IV enables comprehensive analysis revealing molecular basis of disease phenotype.. Novel human cellular model of CDA IV enables comprehensive analysis revealing molecular basis of disease phenotype.
Red blood cell disorders can result in severe anemia. One such disease, congenital dyserythropoietic anemia IV (CDA IV) is caused by heterozygous mutation E325K in the transcription factor KLF1. Howev
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Investigate the effect of gain of HAND2 on chromatin accessibility.
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