RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/34562210http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/34562210http://www.w3.org/2000/01/rdf-schema#comment"The aim of the study was to perform family-based association analysis of PRKCB1, CBLN1 and KCNMB4 gene polymorphisms and autism disorder. We comprised 206 Caucasian children with autistic spectrum disorder (ASD) and their biological parents. In transmission/disequilibrium test we observed that T-allele of the rs198198 polymorphism of the PRKCB1 gene was more often transmitted to affected children in the male subgroup (p = 0.010). Additionally, the T carrier state was significantly associated with hypotonia (p = 0.048). In the female subgroup, the T-allele carriers more often showed more mobile/vital behavior (p = 0.046). In conclusion, our study showed that the rs198198 of the PRKCB1 gene may be associated with ASD in men and with some features characteristic for the disorder."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.org/dc/terms/identifier"doi:10.1007/s10803-021-05291-3"xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Grzeszczak W."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Emich-Widera E."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Iwanicki T."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Gorczynska-Kosiorz S."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Balcerzyk A."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Niemiec P."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Kazek B."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Likus W."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Iwanicka J."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Kapinos M."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Jarosz A."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/author"Kapinos-Gorczyca A."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/name"J Autism Dev Disord"xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/pages"4213-4218"xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/title"Family-Based Cohort Association Study of PRKCB1, CBLN1 and KCNMB4 Gene Polymorphisms and Autism in Polish Population."xsd:string
http://purl.uniprot.org/citations/34562210http://purl.uniprot.org/core/volume"52"xsd:string
http://purl.uniprot.org/citations/34562210http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/34562210
http://purl.uniprot.org/citations/34562210http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/34562210
http://purl.uniprot.org/uniprot/#_P05771-mappedCitation-34562210http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34562210
http://purl.uniprot.org/uniprot/#_P23435-mappedCitation-34562210http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34562210
http://purl.uniprot.org/uniprot/#_Q86W47-mappedCitation-34562210http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/34562210