Now showing items 1-3 of 3

    Issue DateTitleAuthor(s)
    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.
    21 July 2017Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes  Johnson, MB; De Franco, E; Lango Allen, H; et al.