Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome |
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Authors: | Gabriela Petrof,Arti Nanda,Jake Howden,Takuya Takeichi,James  R. McMillan,Sophia Aristodemou,Linda Ozoemena,Lu Liu,Andrew  P. South,Celine Pourreyron,Dimitra Dafou,Laura  E. Proudfoot,Hejab Al-Ajmi,Masashi Akiyama,W.H.  Irwin McLean,Michael  A. Simpson,Maddy Parsons,John  A. McGrath |
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Affiliation: | 1 St. John’s Institute of Dermatology, King’s College London, Guy’s Campus, London SE1 9RT, UK;2 As’ad Al-Hamad Dermatology Center, Al-Sabah Hospital, Kuwait City 13001, Kuwait;3 Randall Division of Cell and Molecular Biophysics, King’s College London, Guy’s Campus, London SE1 9RT, UK;4 Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya 466-8560, Japan;5 National Diagnostic Epidermolysis Bullosa Laboratory, Viapath, St. Thomas’ Hospital, London SE1 7EH, UK;6 Dermatology and Genetic Medicine, College of Life Sciences and College of Medicine, Dentistry, and Nursing, University of Dundee, Dundee DD1 5EH, UK;7 Department of Genetics, Development, and Molecular Biology, School of Biology, Aristotle University, Thessaloniki 54124, Greece;8 Department of Medical and Molecular Genetics, King’s College London School of Medicine and Guy’s Hospital, London SE1 9RT, UK |
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