Sharing of PPT mutations between distinct clinical forms of neuronal ceroid lipofuscinoses in patients from Scotland [4]

P. B. Munroe, N. D E Greene, K. Y. Leung, S. E. Mole, R. M. Gardiner, H. M. Mitchison, J. B P Stephenson, Y. J. Crow

    Research output: Contribution to journalArticlepeer-review

    Original languageEnglish
    Pages (from-to)790
    JournalJournal of Medical Genetics
    Volume35
    Issue number9
    Publication statusPublished - 1998

    Keywords

    • Age of Onset
    • Humans
    • genetics: Mutation
    • genetics: Mutation, Missense
    • genetics: Neuronal Ceroid-Lipofuscinoses
    • Scotland
    • genetics: Thiolester Hydrolases

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