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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...

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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

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