Genes Related to Mitochondrial Functions, Protein Degradation, and Chromatin Folding Are Differentia...
Genes Related to Mitochondrial Functions, Protein Degradation, and Chromatin Folding Are Differentially Expressed in Lymphomonocytes of Rett Syndrome Patients
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Cairo, Egypt: Hindawi Limiteds
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English
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Cairo, Egypt: Hindawi Limiteds
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Rett syndrome (RTT) is mainly caused by mutations in the X-linked methyl-CpG binding protein (MeCP2) gene. By binding to methylated promoters on CpG islands, MeCP2 protein is able to modulate several genes and important cellular pathways. Therefore, mutations in MeCP2 can seriously affect the cellular phenotype. Today, the pathways that MeCP2 mutat...
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Genes Related to Mitochondrial Functions, Protein Degradation, and Chromatin Folding Are Differentially Expressed in Lymphomonocytes of Rett Syndrome Patients
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TN_cdi_doaj_primary_oai_doaj_org_article_f55eb4a6076d48bfa23b5ac4d211ee5c
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f55eb4a6076d48bfa23b5ac4d211ee5c
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ISSN
0962-9351
E-ISSN
1466-1861
DOI
10.1155/2013/137629
