Functional Assessment of a New PBX1 Variant in a 46,XY Fetus with Severe Syndromic Difference of Sexual Development through CRISPR-Cas9 Gene Editing
Laura Mary(Inserm), Sylvie Jaillard(Inserm), Antoine Bigand(Hôpital Pontchaillou), Laurence Cluzeau(Centre Hospitalier Universitaire de Rennes), Delphine Leclerc(Inserm), Marc‐Antoine Belaud‐Rotureau(Inserm), Aurélie Cauchoix(Hôpital Pontchaillou), Séverine Mazaud‐Guittot(Inserm), Philippe Loget(Hôpital Pontchaillou), Bertrand Evrard(Inserm), Anna Lokchine(Inserm), Audrey Labalme(Hospices Civils de Lyon), Stéphane Dréano(Établissement Français du Sang), Pascale Bellaud(Centre National de la Recherche Scientifique), David Gilot(Inserm)
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