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pro vyhledávání: '"Arthur Sorlin"'
Autor:
Anne Miret, Lola Lemasson, Benjamin Cogné, Laurence Perrin, Frédéric Tran Mau-Them, Rémi Mathevet, Marion Boucon, Elise Schaefer, Christel Thauvin-Robinet, Christine Juif, Juliette Piard, Solène Bourgouin, Jenny Cornaton, Bertrand Isidor, Catherine Sarret, Fabienne Prieur, Coralie Gonin-Olympiade, Alexandra Afenjar, Christine Coubes, Boris Keren, Bénédicte Gérard, Catherine Vincent-Delorme, Kim Giraudat, Laurence Faivre, Amélie Piton, Antonio Vitobello, Thomas Smol, Annick Toutain, Arthur Sorlin, Sylvie Odent, Yann Trousselet, Fanny Tessier, Martin Chevarin, David Geneviève, Sébastien Moutton, Anne-Claire Gelineau, Ange-Line Bruel, Claire Nicolas, Aurore Garde, Philippe Khau-Van-Kien, Christophe Philippe, Solveig Heide
Publikováno v:
Clinical Genetics
Clinical Genetics, 2020, ⟨10.1111/cge.13894⟩
Clinical Genetics, Wiley, 2020, ⟨10.1111/cge.13894⟩
Clinical Genetics, 2020, ⟨10.1111/cge.13894⟩
Clinical Genetics, Wiley, 2020, ⟨10.1111/cge.13894⟩
White-Sutton syndrome is a rare developmental disorder characterized by global developmental delay, intellectual disabilities (ID), and neurobehavioral abnormalities secondary to pathogenic pogo transposable element-derived protein with zinc finger d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17d2d648dcff1f210a85420907e1f599
https://hal.science/hal-03124488
https://hal.science/hal-03124488