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Volumn 347, Issue 9010, 1996, Pages 1271-

Different origins of expanded repeats for Haw River syndrome and dentatorubral-pallidoluysian atrophy [26]

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 0029972535     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(96)90796-5     Document Type: Letter
Times cited : (9)

References (5)
  • 1
    • 9044236911 scopus 로고    scopus 로고
    • A unique origin and multistep process for the generation of expanded DRPLA triplet repeats
    • H. Yanagisawa K. Fujii S. Nagafuchi A unique origin and multistep process for the generation of expanded DRPLA triplet repeats Hum Mol Genet 5 1996 373 379
    • (1996) Hum Mol Genet , vol.5 , pp. 373-379
    • Yanagisawa, H.1    Fujii, K.2    Nagafuchi, S.3
  • 2
    • 0028169738 scopus 로고
    • The Haw River syndrome: dentatorubropallidoluysian atrophy(DRPLA) in an African-American family
    • Jr Burke Ms Wingfield Ke Lewis The Haw River syndrome: dentatorubropallidoluysian atrophy(DRPLA) in an African-American family Nat Genet 7 1994 521 524
    • (1994) Nat Genet , vol.7 , pp. 521-524
    • Burke, Jr1    Wingfield, Ms2    Lewis, Ke3
  • 3
    • 0028564730 scopus 로고
    • DNA haplotype analysis of Huntington diease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence
    • F. Squitieri Se Andrew Yp Goldbert DNA haplotype analysis of Huntington diease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence Hum Mol Genet 3 1994 2103 2114
    • (1994) Hum Mol Genet , vol.3 , pp. 2103-2114
    • Squitieri, F.1    Andrew, Se2    Goldbert, Yp3
  • 4
    • 0029080261 scopus 로고
    • Population genetics of trinucleotide repeat polymorphisms
    • Ws Watkins M. Bamshad Lb Jorde Population genetics of trinucleotide repeat polymorphisms Hum Mol Genet 4 1995 1485 1491
    • (1995) Hum Mol Genet , vol.4 , pp. 1485-1491
    • Watkins, Ws1    Bamshad, M.2    Jorde, Lb3
  • 5
    • 0028947051 scopus 로고
    • De novo myotonic dystrophy mutation in a Nigerian kindred
    • R. Krahe M. Eckhardt O. Ogunniyi De novo myotonic dystrophy mutation in a Nigerian kindred Am J Med Genet 56 1995 1067 1074
    • (1995) Am J Med Genet , vol.56 , pp. 1067-1074
    • Krahe, R.1    Eckhardt, M.2    Ogunniyi, O.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.