Cargando...
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...
Gardado en:
| Publicado en: | Comput Math Methods Med |
|---|---|
| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Hindawi Publishing Corporation
2015
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4431600/ https://ncbi.nlm.nih.gov/pubmed/26064184 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/746157 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|