Now showing items 1-3 of 3

    Issue DateTitleAuthor(s)
    3 June 2019Growth disrupting mutations in epigenetic regulatory molecules are associated with abnormalities of epigenetic aging.  Jeffries, AR; Maroofian, R; Salter, CG; et al.
    3 January 2017A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis  Ahmed, MY; Al-Khayat, A; Al-Murshedi, F; et al.
    3 March 2018Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies.  Salter, CG; Beijer, D; Hardy, H; et al.