Mutations involving the sry -related gene sox8 are associated with a spectrum of human reproductive anomalies

HIGHLIGHTS

• who: Selma F. Witchel et al. from the Mutualiste Montsouris, Paris, France, Département d'Anatomie Pathologique, Institut Mutualiste Montsouris, Paris, France, Service d'Endocrinologie, Hôpital Cochin, Paris, France, Biology of Reproduction, CHU Rennes, Rennes, France, Service d'Endocrinologie, Diabétologie et Endocrinologie de la Reproduction, Hôpital Saint-Antoine, Paris, France, Université Paris Descartes and Pediatric Endocrinology Unit, Fondation Ophtalmologique Adolphe de Rothschild, Paris, France, Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy, Laboratory of Endocrine and Metabolic Research and Division of Endocrine and Metabolic Diseases, IRCCS Istituto Auxologico Italiano, Milan . . .
  

   

  

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