RETT SYNDROME; RTT

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Summary

Literature (2)

Literature for OMIM 312750: RETT SYNDROME; RTT

Xenbase Articles:
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Denotes literature images)

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos., Stancheva I,Collins AL,Van den Veyver IB,Zoghbi H,Meehan RR, Mol Cell. August 1, 2003; 12(2):1097-4164.
Rare Diseases of Neurodevelopment: Maintain the Mystery or Use a Dazzling Tool for Investigation? The Case of Rett Syndrome., Cifelli P,Miranda-Lourenço C,De Felice E,Sebastião AM,Diógenes MJ,Aronica E,Ruffolo G,Limatola C,Palma E, Neuroscience. July 15, 2020; 439:1873-7544.

A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos., Stancheva I,Collins AL,Van den Veyver IB,Zoghbi H,Meehan RR, Mol Cell. August 1, 2003; 12(2):1097-4164.

Rare Diseases of Neurodevelopment: Maintain the Mystery or Use a Dazzling Tool for Investigation? The Case of Rett Syndrome., Cifelli P,Miranda-Lourenço C,De Felice E,Sebastião AM,Diógenes MJ,Aronica E,Ruffolo G,Limatola C,Palma E, Neuroscience. July 15, 2020; 439:1873-7544.