Open access
Aug 2026
Reclassification of the GRIA3 splice-site variant in an X-linked family with intellectual disability and psychiatric symptoms
This variant is the first reported, enriching the database and providing additional evidence to support genetic counselling and prenatal diagnosis, and is the first reported to lead to exon 2 skipping of GRIA3.
Lina Hu, Yuqiong Chai, Xiaofei Liu et al.
· Frontiers in Genetics · 0 citations