1-6 of 6
Authors: James A. Poulter
Journal Article
A missense variant in specificity protein 6 (SP6) is associated with amelogenesis imperfecta Open Access
Human Molecular Genetics, Volume 29, Issue 9, 1 May 2020, Pages 1417–1425, https://doi.org/10.1093/hmg/ddaa041
Published: 13 March 2020
Journal Article
Amelogenesis imperfecta caused by N-terminal enamelin point mutations in mice and men is driven by endoplasmic reticulum stress Open Access
Human Molecular Genetics, Volume 26, Issue 10, 15 May 2017, Pages 1863–1876, https://doi.org/10.1093/hmg/ddx090
Published: 11 March 2017
Journal Article
Deletion of amelotin exons 3–6 is associated with amelogenesis imperfecta Open Access
Human Molecular Genetics, Volume 25, Issue 16, 15 August 2016, Pages 3578–3587, https://doi.org/10.1093/hmg/ddw203
Published: 12 July 2016
Journal Article
Deletion of ameloblastin exon 6 is associated with amelogenesis imperfecta Open Access
Human Molecular Genetics, Volume 23, Issue 20, 15 October 2014, Pages 5317–5324, https://doi.org/10.1093/hmg/ddu247
Published: 23 May 2014
Journal Article
A missense mutation in ITGB6 causes pitted hypomineralized amelogenesis imperfecta Open Access
Human Molecular Genetics, Volume 23, Issue 8, 15 April 2014, Pages 2189–2197, https://doi.org/10.1093/hmg/ddt616
Published: 06 December 2013
Journal Article
Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects Open Access
Human Molecular Genetics, Volume 21, Issue 4, 15 February 2012, Pages 776–783, https://doi.org/10.1093/hmg/ddr509
Published: 07 November 2011
