DESCRIBE <http://purl.uniprot.org/citations/24863511>

Subject	Predicate	Object
http://purl.uniprot.org/citations/24863511	http://www.w3.org/1999/02/22-rdf-syntax-ns#type	http://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/24863511	http://www.w3.org/2000/01/rdf-schema#comment	" Unlabelled Mutations in the LRRK2 gene, predominantly G2019S, have been reported in individuals with autosomal dominant inheritance and sporadic Parkinson's disease (PD). The G2019S mutation has an age-dependent penetrance and evidence shows common ancestry. The clinical manifestations are indistinguishable from idiopathic PD. Its prevalence varies according to the population studied ranging from less than 0.1% in Asians to 41% in North African Arabs. This study aimed to identify G2019S mutation in Brazilian idiopathic PD patients. Method We sampled 100 PD patients and 100 age- and gender-matched controls. Genetical analysis was accomplished by polymerase chain reaction (PCR). Results No G2019S mutations were found in both patients with sporadic PD and controls. Conclusions Our results may be explained by the relatively small sample size."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.org/dc/terms/identifier	"doi:10.1590/0004-282x20140019"xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/author	"Barbosa E.R."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/author	"Chien H.F."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/author	"Pereira L.d.a. V."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/author	"Takada L.T."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/author	"Figueiredo T.R."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/author	"Hollaender M.A."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/author	"Tofoli F."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/date	"2014"xsd:gYear
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/name	"Arq Neuropsiquiatr"xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/pages	"356-359"xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/title	"Frequency of the LRRK2 G2019S mutation in late-onset sporadic patients with Parkinson's disease."xsd:string
http://purl.uniprot.org/citations/24863511	http://purl.uniprot.org/core/volume	"72"xsd:string
http://purl.uniprot.org/citations/24863511	http://www.w3.org/2004/02/skos/core#exactMatch	http://purl.uniprot.org/pubmed/24863511
http://purl.uniprot.org/citations/24863511	http://xmlns.com/foaf/0.1/primaryTopicOf	https://pubmed.ncbi.nlm.nih.gov/24863511
http://purl.uniprot.org/uniprot/#_A0A218N881-mappedCitation-24863511	http://www.w3.org/1999/02/22-rdf-syntax-ns#object	http://purl.uniprot.org/citations/24863511
http://purl.uniprot.org/uniprot/#_A2VED2-mappedCitation-24863511	http://www.w3.org/1999/02/22-rdf-syntax-ns#object	http://purl.uniprot.org/citations/24863511
http://purl.uniprot.org/uniprot/#_Q17RV3-mappedCitation-24863511	http://www.w3.org/1999/02/22-rdf-syntax-ns#object	http://purl.uniprot.org/citations/24863511
http://purl.uniprot.org/uniprot/#_Q6MZN9-mappedCitation-24863511	http://www.w3.org/1999/02/22-rdf-syntax-ns#object	http://purl.uniprot.org/citations/24863511
http://purl.uniprot.org/uniprot/#_Q5S007-mappedCitation-24863511	http://www.w3.org/1999/02/22-rdf-syntax-ns#object	http://purl.uniprot.org/citations/24863511
http://purl.uniprot.org/uniprot/A0A218N881	http://purl.uniprot.org/core/mappedCitation	http://purl.uniprot.org/citations/24863511
http://purl.uniprot.org/uniprot/Q5S007	http://purl.uniprot.org/core/mappedCitation	http://purl.uniprot.org/citations/24863511
http://purl.uniprot.org/uniprot/Q17RV3	http://purl.uniprot.org/core/mappedCitation	http://purl.uniprot.org/citations/24863511