Article

Identification of the Presence of a Novel Variant of CC2D1A Linked to Autosomal Recessive Intellectual Disability 3 in an Iranian Family and Investigating the Structure and Pleiotropic Effects of this Gene

2022-12-05

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Intellectual disability (ID) is a major health problem in our society and it is highly heterogeneous and complex. Numerous genes are involved in the development and normal function of the brain and defects in any of them can result in intellectual disability. Considering that many of these genes have not yet been identified, and those that have been identified h...

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Literature Corpus work: 547080f9-301c-5cdf-8958-5badccd046e3
DOI: 10.21203/rs.3.rs-2339774/v1

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