Molecular and phenotypical findings of a novel de novo <i>SYNGAP1</i> gene variant in an 11-year-old Iranian boy with intellectual disability
Atefeh Mir(Isfahan University of Medical Sciences), Mohammad Amin Tabatabaiefar(Isfahan University of Medical Sciences), Hane Lee(Orion Corporation (United Kingdom)), Fahimeh Akbarian(Isfahan University of Medical Sciences), Yongjun Song(Seoul Medical Center), Zakiye Nadeali(Isfahan University of Medical Sciences)
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