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Updated: Oct 17, 2025

A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
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Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders

Joseph T Shieh1,2, Monica Penon-Portmann3,4, Karen H Y Wong5

  • 1Institute for Human Genetics, University of California San Francisco, San Francisco, CA, USA. Joseph.shieh2@ucsf.edu.

NPJ Genomic Medicine
|October 13, 2021
PubMed
Abstract

No abstract available in PubMed .

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