532
Views
0
CrossRef citations to date
0
Altmetric
Case Report

Two Chinese patients of sporadic Creutzfeldt–Jacob disease with a S97N mutation in PRNP gene

, , , , &
Pages 141-144 | Received 08 May 2023, Accepted 24 Oct 2023, Published online: 14 Nov 2023

References

  • Chen C, Dong XP. Epidemiological characteristics of human prion diseases. Infect Diseases Poverty. 2016;5(1):47. PubMed PMID: 27251305; PubMed Central PMCID: PMC4890484. doi: 10.1186/s40249-016-0143-8
  • Kim MO, Takada LT, Wong K, et al. Genetic PrP prion diseases. Cold Spring Harb Perspect Biol. 2018;10(5):a033134. Epub 2017/08/06 PubMed PMID: 28778873; PubMed Central PMCID: PMCPMC5932589. doi: 10.1101/cshperspect.a033134
  • Kovacs GG, Puopolo M, Ladogana A, et al. Genetic prion disease: the EUROCJD experience. Hum Genet. 2005;118(2):166–174. Epub 2005/09/28 PubMed PMID: 16187142. doi: 10.1007/s00439-005-0020-1
  • Shi Q, Chen C, Xiao K, et al. Genetic prion disease: insight from the features and experience of China National surveillance for Creutzfeldt-Jakob disease. Neurosci Bull. 2021;37(11):1570–1582. Epub 2021/09/07 PubMed PMID: 34487324; PubMed Central PMCID: PMCPMC8566684. doi: 10.1007/s12264-021-00764-y
  • Xiao K, Yang XH, Zou WQ, et al. Assessment of the sensitivity and specificity of the established real-time quaking-induced conversion (RT-QuIC) technique in Chinese CJD surveillance. Biomed Environ Sci. 2020;33(8):620–622. Epub 2020/09/17 PubMed PMID: 32933614. doi: 10.3967/bes2020.081
  • Zheng L, Longfei J, Jing Y, et al. PRNP mutations in a series of apparently sporadic neurodegenerative dementias in China. Am J Med Genet B Neuropsychiatr Genet. 2008;147B(6):938–944. Epub 2008/04/22 PubMed PMID: 18425766. doi: 10.1002/ajmg.b.30761
  • Shi Q, Chen C, Xiao K, et al. Characteristics of different types of prion diseases - China’s surveillance. Chin CDC Weekly. 2022;4(33):723–728. Epub 2022/10/27 PubMed PMID: 36285115; PubMed Central PMCID: PMCPMC9547742. doi: 10.46234/ccdcw2022.151