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Pubmed for Handhelds

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Journal Abstract Search

854 related items for PubMed ID: 17274457

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  • 4. A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene.
    Wang D, Wu B, Li Y, Heng W, Zhong H, Mu Y, Wang J.
    J Hum Genet; 2001; 46(3):152-4. PubMed ID: 11310584
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  • 7. Low density lipoprotein receptor (LDLR) gene mutations in Canadian subjects with familial hypercholesterolemia, but not of French descent.
    Wang J, Huff E, Janecka L, Hegele RA.
    Hum Mutat; 2001 Oct; 18(4):359. PubMed ID: 11668627
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  • 13. LDL-receptor mutations in Europe.
    Dedoussis GV, Schmidt H, Genschel J.
    Hum Mutat; 2004 Dec; 24(6):443-59. PubMed ID: 15523646
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  • 14. Familial hypercholesterolemia: epidemiology, Neolithic origins and modern geographic distribution.
    Liyanage KE, Burnett JR, Hooper AJ, van Bockxmeer FM.
    Crit Rev Clin Lab Sci; 2011 Dec; 48(1):1-18. PubMed ID: 21657943
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  • 15. Moderate phenotypic expression of familial hypercholesterolemia in Tunisia.
    Jelassi A, Slimani A, Jguirim I, Najah M, Abid A, Boughamoura L, Mzid J, Fkih M, Maatouk F, Rouis M, Varret M, Slimane MN.
    Clin Chim Acta; 2010 May 02; 411(9-10):735-8. PubMed ID: 20144596
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  • 16. A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia.
    Hopkins PN, Wu LL, Stephenson SH, Xin Y, Katsumata H, Nobe Y, Nakajima T, Hirayama T, Emi M, Williams RR.
    J Hum Genet; 1999 May 02; 44(6):364-7. PubMed ID: 10570905
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  • 17. Common mutations of familial hypercholesterolemia patients in Taiwan: characteristics and implications of migrations from southeast China.
    Chiou KR, Charng MJ.
    Gene; 2012 Apr 25; 498(1):100-6. PubMed ID: 22353362
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  • 19. Familial defective apolipoprotein B-100.
    Hansen PS.
    Dan Med Bull; 1998 Sep 25; 45(4):370-82. PubMed ID: 9777289
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