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RNA sequencing reveals deep intronic CEP120 variant: A report of the diagnostic odyssey for two siblings with Joubert syndrome type 31.

Aren Elizabeth MarshallGabrielle T LemireYijing LiangJorge DavilaMadeline Cousenull nullKym M BoycottKristin D Kernohan
Published in: American journal of medical genetics. Part A (2023)
Keyphrases
  • single cell
  • intellectual disability
  • case report
  • autism spectrum disorder