https://openalex.org/T11772
This cluster of papers focuses on the molecular basis, genetic mutations, and neurological manifestations of Rett syndrome and related disorders such as Fragile X syndrome. It explores the role of MeCP2, synaptic function, autism-like behaviors, and altered brain development in these conditions.
@prefix oasubfields: <https://openalex.org/subfields/> .
@prefix openalex: <https://lambdamusic.github.io/openalex-hacks/ontology/> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
<https://openalex.org/T11772> a skos:Concept ;
rdfs:label "Molecular Basis of Rett Syndrome and Related Disorders"@en ;
rdfs:isDefinedBy openalex: ;
owl:sameAs <https://en.wikipedia.org/wiki/Rett_syndrome>,
<https://openalex.org/T11772> ;
skos:broader oasubfields:1311 ;
skos:definition "This cluster of papers focuses on the molecular basis, genetic mutations, and neurological manifestations of Rett syndrome and related disorders such as Fragile X syndrome. It explores the role of MeCP2, synaptic function, autism-like behaviors, and altered brain development in these conditions."@en ;
skos:inScheme openalex: ;
skos:prefLabel "Molecular Basis of Rett Syndrome and Related Disorders"@en ;
openalex:cited_by_count 1120569 ;
openalex:works_count 44859 .