Works about METHIONINE adenosyltransferase


Results: 24
    1

    Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.

    Published in:
    Orphanet Journal of Rare Diseases, 2015, v. 10, n. 1, p. 1, doi. 10.1186/s13023-015-0321-y
    By:
    • Yin-Hsiu Chien;
    • Abdenur, Jose E.;
    • Baronio, Federico;
    • Bannick, Allison Anne;
    • Corrales, Fernando;
    • Couce, Maria;
    • Donner, Markus G.;
    • Ficicioglu, Can;
    • Freehauf, Cynthia;
    • Frithiof, Deborah;
    • Gotway, Garrett;
    • Koichi Hirabayashi;
    • Hofstede, Floris;
    • Hoganson, George;
    • Wuh-Liang Hwu;
    • James, Philip;
    • Sook Kim;
    • Korman, Stanley H.;
    • Lachmann, Robin;
    • Levy, Harvey
    Publication type:
    Article
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