Absence of association between Two HECTD2 polymorphisms and sporadic Creutzfeldt-Jakob disease

Dementia and Geriatric Cognitive Disorders

Volumn 31, Issue 2, 2011, Pages 146-151

  Jeong, Byung Hoon ^a   Lee, Kyung Hee ^b   Lee, Yun Jung ^a   Yun, Jisuk ^a   Park, Young Jae ^a   Cho, Han Jeong ^a   Kim, Young Hoon ^b   Cho, Young Sook ^b   Choi, Eun Kyoung ^a   Carp, Richard I ^c   Kim, Yong Sun ^a  

^a Hallym University   (South Korea)

^b Samkwang Medical Laboratories   (South Korea)

^c NEW YORK STATE INSTITUTE FOR BASIC RESEARCH IN DEVELOPMENTAL DISABILITIES   (United States)

Author keywords

Creutzfeldt Jakob disease; E3 ubiquitin ligase; Homologous to E6 AP carboxyl terminus E3 ubiquitin ligase D2; Population genetics; Prion disease; Single nucleotide polymorphism

Indexed keywords

GENOMIC DNA; PROTEIN HECTD2; UBIQUITIN PROTEIN LIGASE E3; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CODON; CONTROLLED STUDY; FEMALE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; INTRON; KOREA; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PROMOTER REGION; SINGLE NUCLEOTIDE POLYMORPHISM; SPORADIC CREUTZFELDT JAKOB DISEASE;

AGED; ALLELES; CREUTZFELDT-JAKOB SYNDROME; DNA; FEMALE; GENE FREQUENCY; GENOTYPE; HAPLOTYPES; HUMANS; MALE; MIDDLE AGED; POLYMORPHISM, GENETIC; REPUBLIC OF KOREA; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; UBIQUITIN-PROTEIN LIGASES;

EID: 79951569249     PISSN: 14208008     EISSN: None     Source Type: Journal    
DOI: 10.1159/000324133     Document Type: Article

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