Changes in the Cerebrospinal Fluid and Plasma Lipidome in Patients with Rett Syndrome
Changes in the Cerebrospinal Fluid and Plasma Lipidome in Patients with Rett Syndrome
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Switzerland: MDPI AG
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Language
English
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Publisher
Switzerland: MDPI AG
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Rett syndrome (RTT) is defined as a rare disease caused by mutations of the methyl-CpG binding protein 2 (MECP2). It is one of the most common causes of genetic mental retardation in girls, characterized by normal early psychomotor development, followed by severe neurologic regression. Hitherto, RTT lacks a specific biomarker, but altered lipid hom...
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Changes in the Cerebrospinal Fluid and Plasma Lipidome in Patients with Rett Syndrome
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TN_cdi_doaj_primary_oai_doaj_org_article_64194d3322854e6aa3836f9cb85ae727
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_64194d3322854e6aa3836f9cb85ae727
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ISSN
2218-1989
E-ISSN
2218-1989
DOI
10.3390/metabo12040291