Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of families
Alexandre Rouen(National Institutes of Health), Sophie Christin‐Maître(Sorbonne Université), V. Kerlan(Centre Hospitalier Régional Universitaire de Brest), Catherine Pienkowski(Centre Hospitalier Universitaire de Toulouse), Sophie Catteau-Jonard(Inserm), A.M. Guedj(Centre Hospitalier Universitaire de Nîmes), Brigitte Delemer(Centre Hospitalier Universitaire de Reims), Philippe Touraine(Sorbonne Université), Eli Rogers(Inserm), Virginie Grouthier(Centre Hospitalier Universitaire de Bordeaux), Thierry Brue(Inserm), Sandra Chantot‐Bastaraud(Fondation de Rothschild), Tabassome Simon(Sorbonne Université), Alexandra Rousseau(Houston Methodist), Anne Gompel(Délégation Paris 5), Esther Kott(Inserm), Anne Bachelot, Yves Reznik(Centre Hospitalier Universitaire de Caen Normandie), Isabelle Cédrin(Hôpital Jean-Verdier), Jean‐Pierre Siffroi(Sorbonne Université)
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