Now showing items 1-3 of 3

    Issue DateTitleAuthor(s)
    20 February 2013Identification of a SLC19A2 nonsense mutation in Persian families with thiamine-responsive megaloblastic anemia  Setoodeh, A; Haghighi, A; Saleh-Gohari, N; et al.
    15 February 2018Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome  Habeb, AM; Flanagan, SE; Zulali, MA; et al.
    4 May 2017Recessively inherited LRBA mutations cause autoimmunity presenting as neonatal diabetes  Johnson, MB; De Franco, E; Lango Allen, H; et al.