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Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease

Rett Syndrome (RTT) is a severe, rare, and progressive developmental disorder with patients displaying neurological regression and autism spectrum features. The affected individuals are primarily young females, and more than 95% of patients carry de novo mutation(s) in the Methyl-CpG-Binding Protein...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Biomolecules
Päätekijät: Pejhan, Shervin, Rastegar, Mojgan
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: MDPI 2021
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7827577/
https://ncbi.nlm.nih.gov/pubmed/33429932
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biom11010075
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