Defective axon guidance links H3K4 deregulation to neurodevelopment disorder
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE143811
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RNA sequencing (mRNAs) of N2 and two set-2 mutant set-2(tm1630) and set-2(zr2012) during mid-embryogenesis Examination of the effect on the transcriptional landscape when removing set-2 a H3K4 methyltransferase. Three samples pr. genotype. Sample name with prefix 2 was run in a seperate experiment
创建时间：
2020-08-24
