A novel variant in the 3′ UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding - Concepedia

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A novel variant in the 3′ UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding

29

Citations

36

References

2014

Year

Tao Zeng, Zhaofei Dong, Shujing Liu, Rui-Ping Wan, Ling-Jia Tang, Ting Liu, Qi‐Hua Zhao, Yi‐Wu Shi, Yong‐Hong Yi, Wei‐Ping Liao,

Novel VariantTranscriptional RegulationGenetic DisorderGeneticsGene RegulationMolecular GeneticsGapdh ’Human Scn1a GeneGene ExpressionMedicineCell BiologyRna Processing

References

	Year	Citations

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