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Journal Abstract Search

208 related items for PubMed ID: 15971231

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  • 2. Detection of C1 inhibitor (SERPING1/C1NH) mutations in exon 8 in patients with hereditary angioedema: evidence for 10 novel mutations.
    Blanch A, Roche O, López-Granados E, Fontán G, López-Trascasa M.
    Hum Mutat; 2002 Nov; 20(5):405-6. PubMed ID: 12402344
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  • 5. Mutation screening of the C1 inhibitor gene among Hungarian patients with hereditary angioedema.
    Kalmár L, Bors A, Farkas H, Vas S, Fandl B, Varga L, Füst G, Tordai A.
    Hum Mutat; 2003 Dec; 22(6):498. PubMed ID: 14635117
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  • 7. Analysis of SERPING1 expression on hereditary angioedema patients: quantitative analysis of full-length and exon 3 splicing variants.
    de la Cruz RM, López-Lera A, López-Trascasa M.
    Immunol Lett; 2012 Jan 30; 141(2):158-64. PubMed ID: 22001489
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  • 10. SERPING1 mutations in 59 families with hereditary angioedema.
    López-Lera A, Garrido S, Roche O, López-Trascasa M.
    Mol Immunol; 2011 Oct 30; 49(1-2):18-27. PubMed ID: 21864911
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  • 13. Paternal mosaicism and hereditary angioedema in a Taiwanese family.
    Yu TC, Shyur SD, Huang LH, Wen DC, Li JS.
    Ann Allergy Asthma Immunol; 2007 Oct 30; 99(4):375-9. PubMed ID: 17941288
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  • 16. Familial adenomatous polyposis: aberrant splicing due to missense or silent mutations in the APC gene.
    Aretz S, Uhlhaas S, Sun Y, Pagenstecher C, Mangold E, Caspari R, Möslein G, Schulmann K, Propping P, Friedl W.
    Hum Mutat; 2004 Nov 30; 24(5):370-80. PubMed ID: 15459959
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