Human Genome Epidemiology Literature Finder
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Query Trace: Epilepsy and CC2D2A[original query] |
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New insights into CC2D2A-related Joubert syndrome. Journal of medical genetics 2022 11 . Harion Madeleine, Qebibo Leila, Riquet Audrey, Rougeot Christelle, Afenjar Alexandra, Garel Catherine, Louha Malek, Lacaze Emmanuelle, Audic-Gérard Frédérique, Barth Magali, Berquin Patrick, Bonneau Dominique, Bourdain Frédéric, Busa Tiffany, Colin Estelle, Cuisset Jean-Marie, Des Portes Vincent, Dorison Nathalie, Francannet Christine, Héron Bénédicte, Laroche Cécile, Lebrun Marine, Métreau Julia, Odent Sylvie, Pasquier Laurent, Trujillo Yaumara Perdomo, Perrin Laurine, Pinson Lucile, Rivier François, Sigaudy Sabine, Thauvin-Robinet Christel, Louvier Ulrike Walther, Labayle Olivier, Rodriguez Diana, Valence Stéphanie, Burglen Lyd |
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- Page last updated:Apr 22, 2024
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