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SLC35F1 as a candidate gene for neurodevelopmental disorders resembling Rett syndrome.

Elisabetta Di FedeAngela PeronElisa Adele ColomboCristina GervasiniAglaia Vignoli
Published in: American journal of medical genetics. Part A (2021)
Keyphrases
  • copy number
  • genome wide
  • case report
  • genome wide identification
  • congenital heart disease