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A novel variant in the 3′ UTR of humanSCN1Agene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH’s binding

✍ Scribed by Zeng, Tao; Dong, Zhao-Fei; Liu, Shu-Jing; Wan, Rui-Ping; Tang, Ling-Jia; Liu, Ting; Zhao, Qi-Hua; Shi, Yi-Wu; Yi, Yong-Hong; Liao, Wei-Ping; Long, Yue-Sheng


Book ID
121565877
Publisher
Springer
Year
2014
Tongue
English
Weight
609 KB
Volume
133
Category
Article
ISSN
0340-6717

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