Structural, Dynamical, and Energetical Consequences of Rett Syndrome Mutation R133C in MeCP2

Rett Syndrome (RTT) is a progressive neurodevelopmental disease affecting females. RTT is caused by mutations in the MECP2 gene and various amino acid substitutions have been identified clinically in different domains of the multifunctional MeCP2 protein encoded by this gene. The R133C variant in th...

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Detalles Bibliográficos
Autores principales: Kucukkal, Tugba G., Alexov, Emil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431600/
https://www.ncbi.nlm.nih.gov/pubmed/26064184
http://dx.doi.org/10.1155/2015/746157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4431600/
https://www.ncbi.nlm.nih.gov/pubmed/26064184
http://dx.doi.org/10.1155/2015/746157

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