A STAG3 missense mutation in two sisters with primary ovarian insufficiency

Roberto Colombo1, Alessandro Pontoglio2, Maurizio Bini3

  • 1Center for the Study of Rare Hereditary Diseases, Niguarda Ca' Granda Metropolitan Hospital, Milan, Italy; Institute of Clinical Biochemistry, Faculty of Medicine, Catholic University of the Sacred Heart, Policlinico Agostino Gemelli, Rome, Italy.

Abstract

No abstract available in PubMed .

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