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Smith, C orcid.org/0000-0001-8320-5105, Whitehouse, L, Poulter, J orcid.org/0000-0003-2048-5693 et al. (8 more authors) (2020) A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfecta. Human Molecular Genetics. ISSN 0964-6906

Brookes, SJ orcid.org/0000-0002-9097-7311, Barron, MJ, Smith, CEL orcid.org/0000-0001-8320-5105 et al. (7 more authors) (2017) Amelogenesis Imperfecta caused by N-Terminal Enamelin Point Mutations in Mice and Men is driven by Endoplasmic Reticulum Stress. Human Molecular Genetics, 26 (10). ISSN 0964-6906

This list was generated on Mon Jul 6 00:54:37 2020 BST.