Article info

Original research
SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum

Authors

  1. Correspondence to Professor Enza Maria Valente, Department of Molecular Medicine, University of Pavia, Pavia, Lombardia, Italy; enzamaria.valente{at}unipv.it
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Citation

Serpieri V, D’Abrusco F, Dempsey JC University of Washington Center for Mendelian Genomics (UW-CMG) group, et al
SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum

Publication history

  • Received July 30, 2021
  • Accepted September 29, 2021
  • First published October 21, 2021.

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    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

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