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Volumn 16, Issue 7, 2008, Pages 869-872

Conservation of 5′-upstream region of the FBN1 gene in primates

Author keywords

[No Author keywords available]

Indexed keywords

FIBRILLIN 1; GENOMIC DNA; NUCLEOTIDE; TRANSCRIPTION FACTOR; ACTIN BINDING PROTEIN; FIBRILLIN;

EID: 45749116956     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2008.51     Document Type: Article
Times cited : (2)

References (11)
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    • Localization of the fibrillin (FBN) gene to chromosome 15, band q21.1
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    • A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features af the Marfan syndrome
    • Milewicz DM, Grossfield J, Cao SN, Kielty C, Covitz W, Jewett T: A mutation in FBN1 disrupts profibrillin processing and results in isolated skeletal features af the Marfan syndrome. J Clin Invest 1995; 95: 2373-2378.
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  • 8
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    • An analysis of vertebrate mINA sequences: Intimations of translational control
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    • Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.