Expanding the Phenotypic Spectrum of the Recurrent De Novo FBXO31 p. Asp334Asn Variant: Evidence for a Novel Neurodevelopmental Disorder (Kruer Syndrome)

Fuente: Wiley Open Access

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Bibliographic Details
Main Authors:	Carolina I. Galaz‐Montoya, Sara A. Lewis, Maureen K. Galindo, Patricia Cornejo, Peter T. Skidmore, Pritha Bisarad, Helen Magee, Kelly Bontempo, Boris Keren, Alexandra Afenjar, Matej Skorvanek, Michael Zech, Ingrid M. Wentzensen, Christina A. Gurnett, Wendy K. Chung, Somayeh Bakhtiari, Michael C. Kruer
Format:	Artículo Open Access
Published:	Wiley 2026
Subjects:	Clinical Genetics
Online Access:	Acceder al recurso
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