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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

238 related items for PubMed ID: 1975493

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  • 23. Homology modeling of human methylmalonyl-CoA mutase: a structural basis for point mutations causing methylmalonic aciduria.
    Thomä NH, Leadlay PF.
    Protein Sci; 1996 Sep; 5(9):1922-7. PubMed ID: 8880917
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  • 25. [Molecular diagnosis of a kindred with novel mutation of methylmalonyl-CoA mutase gene using non-RI SSCP].
    Toyo-Oka Y, Wada C, Ohnuki Y, Takada F, Ohtani H.
    Rinsho Byori; 1995 Jun; 43(6):625-9. PubMed ID: 7602808
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  • 32. Novel mutations in a Thai patient with methylmalonic acidemia.
    Champattanachai V, Ketudat Cairns JR, Shotelersuk V, Keeratichamroen S, Sawangareetrakul P, Srisomsap C, Kaewpaluek V, Svasti J.
    Mol Genet Metab; 2003 Aug; 79(4):300-2. PubMed ID: 12948746
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  • 35. Identification of two novel mutations in the methylmalonyl-CoA mutase gene with decreased levels of mutant mRNA in methylmalonic acidemia.
    Ogasawara M, Matsubara Y, Mikami H, Narisawa K.
    Hum Mol Genet; 1994 Jun; 3(6):867-72. PubMed ID: 7951229
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  • 38. Isolated methylmalonic acidemia: a case report.
    Es Sadki T, Badiou S, Boubal M, Baleine J, Sieso V, Vallat C, Cristol JP, Vianey-Saban C, Cambonie G.
    Ann Biol Clin (Paris); 2016 Aug 01; 74(4):472-6. PubMed ID: 27492701
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