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Article

Carrier Testing in Known Autosomal Recessive Intellectual Disability Genes in an Iranian Healthy Individual Using Exome Sequencing.

Archives of Iranian medicine - 1 Oct 2015

Mehrjoo Zohreh, Akbari Mohammad Reza, Abedini Seyedeh Sedigheh, Vaziri Saeideh, Kahrizi Kimia, Najmabadi Hossein

Abstract excerpt

BACKGROUND: Intellectual Disability (ID) is one of the most common disabling impairments worldwide. Autosomal recessive ID (ARID), a genetically heterogeneous disorder, is more common in countries such as Iran where the rate of consanguineous marriages is high. Considering the social-economic burden of ARID in our country, it is crucial to find out whether couples who are cousins are carriers for disease causing...

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Identifiers

PMID: 26443248
DOI: 0151810/AIM.006

Genes

PMM2
RBM28

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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