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dc.creatorDimitrijević, Rajna
dc.creatorCadez, Ivana
dc.creatorKeckarević-Marković, Milica
dc.creatorKeckarević, Dušan
dc.creatorKecmanović, Miljana
dc.creatorDobričić, Valerija
dc.creatorSavić-Pavićević, Dušanka
dc.creatorBrajusković, Goran
dc.creatorRomac, Stanka
dc.date.accessioned2021-02-18T10:35:21Z
dc.date.available2021-02-18T10:35:21Z
dc.date.issued2010
dc.identifier.issn0020-7454
dc.identifier.urihttp://intor.torlakinstitut.com/handle/123456789/299
dc.description.abstractPrion diseases are a group of etiologically heterogenous neurodegenerative disorders. We have analyzed the coding region of PRNP gene in 121 healthy citizens of Serbia to determine whether the frequencies of M129V, E219K, and octapeptide repeat number polymorphism. For Serbian population, polymorphism of PRNP gene at codon 129 does not differ from healthy European populations. Also codon 219 is monomorphic for the Glu allele both in Serbian population and other European populations. On the contrary, in Serbian population we did not detect any deletions or insertions in octapeptide repeat region, whereas deletions were detected in other European populations.en
dc.publisherTaylor & Francis Ltd, Abingdon
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/143013/RS//
dc.rightsrestrictedAccess
dc.sourceInternational Journal of Neuroscience
dc.subjectE219Ken
dc.subjectM129Ven
dc.subjectpolymorphismen
dc.subjectprion diseasesen
dc.subjectPRNPen
dc.subjectSerbian populationen
dc.titlePolymorphisms of the Prion Protein Gene (PRNP) in a Serbian Populationen
dc.typearticle
dc.rights.licenseARR
dc.citation.epage501
dc.citation.issue7
dc.citation.other120(7): 496-501
dc.citation.rankM23
dc.citation.spage496
dc.citation.volume120
dc.identifier.doi10.3109/00207451003765907
dc.identifier.pmid20583902
dc.identifier.rcubconv_254
dc.identifier.scopus2-s2.0-77954180773
dc.identifier.wos000279487800005
dc.type.versionpublishedVersion


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