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Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder

Tayyaba Afsar1,2, Hongxia Fu3, Hammal Khan4

  • 1Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia.

Frontiers in Genetics
|January 29, 2024
PubMed

Keywords:
SLITRK2developmental anomalyneurodevelopmental disordersnonsense mutationnovel mutationwhole-exome sequencing

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