Wolcott-Rallison syndrome: Pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3

Karen Piper Hanley, Neil Hanley, S. Brickwood, D. T. Bonthron, L. I. Al-Gazali, K. Piper, T. Hearn, D. I. Wilson, Neil A. Hanley

    Research output: Contribution to journalArticlepeer-review

    Original languageEnglish
    Pages (from-to)685-689
    Number of pages4
    JournalJournal of Medical Genetics
    Volume40
    Issue number9
    Publication statusPublished - 1 Sept 2003

    Keywords

    • genetics: Abnormalities, Multiple
    • Base Sequence
    • pathology: Bone Diseases, Developmental
    • Child, Preschool
    • Consanguinity
    • chemistry: DNA
    • DNA Mutational Analysis
    • pathology: Diabetes Mellitus, Type 1
    • Family Health
    • Fatal Outcome
    • Female
    • Humans
    • Infant
    • Infant, Newborn
    • Male
    • Mutation
    • Syndrome
    • genetics: eIF-2 Kinase

    Cite this