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Updated: May 28, 2026

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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Update on the Clinical and Molecular Characterization of Noonan Syndrome and Other RASopathies: A Retrospective Study

Giuseppe Reynolds1,2, Andrea Gazzin2,3, Diana Carli4

  • 1Department of Public Health and Pediatrics, Postgraduate School of Pediatrics, University of Torino, 10126 Turin, Italy.

International Journal of Molecular Sciences
|May 7, 2025
PubMed
Abstract

Keywords:
PTPN11RAF1RAS/MAPK pathwaySOS1congenital disorders

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