Spectrum of Clinical Manifestations in Children With WT1 Mutation: Case Series and Literature Review

BackgroundMutations of the Wilms tumor suppressor-1 gene (WT1) are associated with life-threatening glomerulopathy, disorders of sexual development, Wilm's tumor, and gonadal malignancies. Our objectives were to describe the clinical presentations, age of progression, and onset of complications...

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Main Authors: Patricia Arroyo-Parejo Drayer (Author), Wacharee Seeherunvong (Author), Chryso P. Katsoufis (Author), Marissa J. DeFreitas (Author), Tossaporn Seeherunvong (Author), Jayanthi Chandar (Author), Carolyn L. Abitbol (Author)
Format: Book
Published: Frontiers Media S.A., 2022-04-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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