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De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies

  • Richard J. Holt
  • , Rodrigo M. Young
  • , Berta Crespo
  • , Fabiola Ceroni
  • , Cynthia J. Curry
  • , Emanuele Bellacchio
  • , Dorine A. Bax
  • , Andrea Ciolfi
  • , Marleen Simon
  • , Christina R. Fagerberg
  • , Ellen van Binsbergen
  • , Alessandro De Luca
  • , Luigi Memo
  • , William B. Dobyns
  • , Alaa Afif Mohammed
  • , Samuel J.H. Clokie
  • , Celia Zazo Seco
  • , Yong Hui Jiang
  • , Kristina P. Sørensen
  • , Helle Andersen
    • Jennifer Sullivan, Zöe Powis, Anna Chassevent, Constance Smith-Hicks, Slavé Petrovski, Thalia Antoniadi, Vandana Shashi, Bruce D. Gelb, Stephen W. Wilson, Dianne Gerrelli, Marco Tartaglia, Nicolas Chassaing, Patrick Calvas, Nicola K. Ragge*
*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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Biochemistry, Genetics and Molecular Biology