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Article

A novel heterozygous truncating variant in the AGO1 gene in an Iranian family with schizophrenia as an unreported symptom.

Annals of human genetics - 1 Nov 2023

Mir Atefeh, Khorram Erfan, Song Yongjun, Lee Hane, Tabatabaiefar Mohammad Amin

Abstract excerpt

Intellectual disability (ID) and autism spectrum disorders (ASDs) are the most common developmental disorders in humans. Combined, they affect between 3% and 5% of the population. Although high-throughput genomic methods are rapidly increasing the pool of ASD genes, many cases remain idiopathic. AGO1 is one of the less-known genes related to ID/ASD. This gene encodes a core member protein of the RNA-induced...

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Identifiers

PMID: 37589173
DOI: 10.1111/ahg.12524

Genes

AGO1

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