RETT SYNDROME, CONGENITAL VARIANT

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Summary

Literature (2)

Literature for OMIM 613454: RETT SYNDROME, CONGENITAL VARIANT

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.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. October 13, 2023; :1552-5015.

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.

Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. October 13, 2023; :1552-5015.