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Journal Abstract Search

310 related items for PubMed ID: 12872264

  • 21. Identification and molecular analysis of two apoB gene mutations causing low plasma cholesterol levels.
    Welty FK, Ordovas J, Schaefer EJ, Wilson PW, Young SG.
    Circulation; 1995 Oct 15; 92(8):2036-40. PubMed ID: 7554178
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  • 22. Familial hypobetalipoproteinemia: analysis of three Spanish cases with two new mutations in the APOB gene.
    Martín-Morales R, García-Díaz JD, Tarugi P, González-Santos P, Saavedra-Vallejo P, Magnolo L, Mesa-Latorre JM, di Leo E, Valdivielso P.
    Gene; 2013 Nov 15; 531(1):92-6. PubMed ID: 24001780
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  • 23. [Familial hypobetalipoproteinemia].
    Sobra J, Horínek A, Ceska R, Procházková R, Kvasilová M.
    Cas Lek Cesk; 1997 Feb 12; 136(4):115-9. PubMed ID: 9221181
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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Burnett JR, Hooper AJ, Hegele RA.
    ; 1993 Feb 12. PubMed ID: 33983694
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  • 34. Mental retardation and ataxia due to normotriglyceridemic hypobetalipoproteinemia.
    Homer VM, George PM, du Toit S, Davidson JS, Wilson CJ.
    Ann Neurol; 2005 Jul 12; 58(1):160-3. PubMed ID: 15984016
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  • 36. High frequency of APOB gene mutations causing familial hypobetalipoproteinaemia in patients of Dutch and Spanish descent.
    Fouchier SW, Sankatsing RR, Peter J, Castillo S, Pocovi M, Alonso R, Kastelein JJ, Defesche JC.
    J Med Genet; 2005 Apr 12; 42(4):e23. PubMed ID: 15805152
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  • 38. Novel mutations in abetalipoproteinaemia and homozygous familial hypobetalipoproteinaemia.
    Vongsuvanh R, Hooper AJ, Coakley JC, Macdessi JS, O'Loughlin EV, Burnett JR, Gaskin KJ.
    J Inherit Metab Dis; 2007 Nov 12; 30(6):990. PubMed ID: 18027103
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