A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

Hanadi A. Abdelrahman, Aisha M. Al-Shamsi, Bassam R. Ali, Lihadh Al-Gazali

Research output: Contribution to journalLetterpeer-review

24 Citations (Scopus)
Original languageEnglish
Pages (from-to)586-587
Number of pages2
JournalClinical Genetics
Issue number6
Publication statusPublished - Dec 2018

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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