메뉴 건너뛰기




Volumn 14, Issue 4, 2000, Pages 257-263

The status of SCA1, MJD/SCA3, FRDA, DRPLA and MD triplet containing genes in patients with huntington disease and healthy controls

Author keywords

Expansion; Mutant alleles; PCR analyses; Trinucleotide repeats

Indexed keywords

ARTICLE; CONTROLLED STUDY; DEGENERATIVE DISEASE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; HUMAN; HUNTINGTON CHOREA; NEUROMUSCULAR DISEASE; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT;

EID: 0034444073     PISSN: 01677063     EISSN: None     Source Type: Journal    
DOI: 10.3109/01677060009084502     Document Type: Article
Times cited : (9)

References (12)
  • 1
    • 0032065590 scopus 로고    scopus 로고
    • Laboratory guidelines for Huntington Disease Testing
    • ACMG/ASHG (1998). Laboratory guidelines for Huntington Disease Testing. Am. J. Hum. Genet. 62(5), 1243-1247.
    • (1998) Am. J. Hum. Genet. , vol.62 , Issue.5 , pp. 1243-1247
  • 3
    • 0345337323 scopus 로고    scopus 로고
    • Improved plymerase chain reaction conditions for quick diagnosis of Huntington disease
    • Culjkovic, B., Ruzdijic, S., Rakic, Lj., and Romac, S. (1997). Improved plymerase chain reaction conditions for quick diagnosis of Huntington disease. Brain. Res. Prot., 2, 44-46.
    • (1997) Brain. Res. Prot. , vol.2 , pp. 44-46
    • Culjkovic, B.1    Ruzdijic, S.2    Rakic, Lj.3    Romac, S.4
  • 5
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable in Huntington's disease chromosomes
    • Huntington Disease Collaborative Research Group. (1993). A novel gene containing a trinucleotide repeat that is expanded and unstable in Huntington's disease chromosomes. Cell, 72, 971-83.
    • (1993) Cell , vol.72 , pp. 971-983
  • 6
    • 0032718877 scopus 로고    scopus 로고
    • Possible association between schizophrenia and CAG repeat polymorphism in the spinocerebellar ataxia type 1 (SCA1) gene on human chromosome 6p23
    • Joo, E.J., Lee, J.H., Cannon, T.D., and Price, R.A. (1999). Possible association between schizophrenia and CAG repeat polymorphism in the spinocerebellar ataxia type 1 (SCA1) gene on human chromosome 6p23. Psychistr. Genet., 9, 7-11.
    • (1999) Psychistr. Genet. , vol.9 , pp. 7-11
    • Joo, E.J.1    Lee, J.H.2    Cannon, T.D.3    Price, R.A.4
  • 8
    • 0027521860 scopus 로고
    • The haplotype-relative-risk (HRR) method for analysis of association in nuclear families
    • Knapp, M., Seuchter, S.A. and Baur, M.P. (1993). The haplotype-relative-risk (HRR) method for analysis of association in nuclear families. Am. J. Hum. Genet., 52, 1085-1093.
    • (1993) Am. J. Hum. Genet. , vol.52 , pp. 1085-1093
    • Knapp, M.1    Seuchter, S.A.2    Baur, M.P.3
  • 9
    • 0026767610 scopus 로고
    • Dynamic mutations: A new class of mutations causing human disease
    • Richards, R.I. and Sutherland, G.R. (1992). Dynamic mutations: a new class of mutations causing human disease. Cell, 70, 709-12.
    • (1992) Cell , vol.70 , pp. 709-712
    • Richards, R.I.1    Sutherland, G.R.2
  • 11
    • 0006675549 scopus 로고
    • Cary, NC: SAS Institute
    • SAS STAT (1991). User Guide(Cary, NC: SAS Institute).
    • (1991) User Guide


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.