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Identification of a novel de novo mutation in the CTNNB1 gene in an Iranian patient with intellectual disability

Published Online: 2022-01-31

Published Print: 2022-04

Authors

Dashti, Sepide

Salehpour, Shadab https://orcid.org/0000-0002-0277-809X
Ghasemi, Mohammad-Reza https://orcid.org/0000-0002-3183-5495
Sadeghi, Hossein https://orcid.org/0000-0001-9599-6151
Rostami, Masoumeh

Hashemi-Gorji, Farzad https://orcid.org/0000-0002-9996-9406
Mirfakhraie, Reza https://orcid.org/0000-0003-1709-8975
Yassaee, Vahid Reza https://orcid.org/0000-0002-1879-3905
Miryounesi, Mohammad https://orcid.org/0000-0003-4705-3794
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Text and Data Mining valid from 2022-01-31

Version of Record valid from 2022-01-31
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Article History

Received: 19 April 2021

Accepted: 14 January 2022

First Online: 31 January 2022

Declarations

:

: This study was approved by the Research Ethics Committee of the Faculty of Medicine, Shahid Beheshti University of Medical Sciences, and was conducted in accordance with the tenets of the Declaration of Helsinki. Informed consent was obtained from parents.

: All the contributing authors agreed for the publication in this journal.

: The authors declare no competing interests.

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