Mitochondrial Proteome Changes in Rett Syndrome

SIMPLE SUMMARY: Rett syndrome (RTT) is a genetic disorder caused by mutations in the X-chromosome. These mutations distort the function of a protein (methyl-CpG-binding protein 2), which controls the expression of several other genes. The resulting pathology, which manifests mostly in female patient...

Descripción completa

Detalles Bibliográficos
Autores principales: Golubiani, Gocha, van Agen, Laura, Tsverava, Lia, Solomonia, Revaz, Müller, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376342/
https://www.ncbi.nlm.nih.gov/pubmed/37508386
http://dx.doi.org/10.3390/biology12070956

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376342/
https://www.ncbi.nlm.nih.gov/pubmed/37508386
http://dx.doi.org/10.3390/biology12070956

Ejemplares similares