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Volumn 46, Issue 8 I, 2000, Pages 1183-1185

Identification of two LDL-receptor mutations causing familial hypercholesterolemia in Indian subjects by a simplified rapid PCR-heteroduplex method

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CROSS LINKING; EXON; FAMILIAL HYPERCHOLESTEROLEMIA; GENE AMPLIFICATION; GENE FREQUENCY; GENE INSERTION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; INDIA; METHODOLOGY; POINT MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS;

EID: 0033882026     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/46.8.1183     Document Type: Article
Times cited : (12)

References (17)
  • 1
    • 0000710395 scopus 로고
    • Familial hypercholesterolemia
    • Scriver CR, Beaudet AL, Sly WS, Valle B, eds. The metabolic bases of inherited diseases, 7th ed. New York: McGraw-Hill
    • (1995) , vol.2 , pp. 1980-2037
    • Goldstein, J.L.1    Hobbs, H.H.2    Brown, M.S.3
  • 6
    • 0008417892 scopus 로고
    • Setting down roots: Indian migrants in South Africa Johannesburg, South Africa: Witwatersrand University Press
    • (1990) , pp. 15-43
    • Bhana, S.1    Brain, J.2
  • 10
    • 0001818958 scopus 로고
    • Familial hypercholesterolemia
    • Durrington PN, ed Hyperlipidaemia: diagnosis and management. London: Butterworth and Co.
    • (1989) , pp. 91-113
    • Durrington, P.N.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.