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Contribution of Iran in Elucidating the Genetic Causes of Autosomal Recessive Intellectual Disability.

Archives of Iranian medicine - 1 Aug 2019

Ataei Reza, Khoshbakht Shahrouz, Beheshtian Maryam, Abedini Seyedeh Sedigheh, Behravan Hanieh, Esmaeili Dizghandi Saeed, Godratpour Fatemeh, Mirzaei Sepide, Bahrami Fatemeh, Akbari Mojdeh, Keshavarzi Fatemeh, Kahrizi Kimia, Najmabadi Hossein

Abstract excerpt

Many genes with different inheritance modes contribute to the pathogenicity of intellectual disability (ID) making it the most known genetically heterogeneous disorder. Advanced next-generation sequencing (NGS) technologies have helped researchers identify genes underlying ID at an exponential pace. As a consanguineous country, Iran is a hotspot for discovering novel autosomal recessive intellectual disability...

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PMID: 31679349

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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