The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (<i>ARMC3</i>)

The Expansion of the Spectrum in Stuttering Disorders to a Novel ARMC Gene Family (<i>ARMC3</i>)

Stuttering is a common neurodevelopment speech disorder that negatively affects the socio-psychological dimensions of people with disability. It displays many attributes of a complex genetic trait, and a few genetic loci have been identified through linkage studies. Stuttering is highly variable reg...

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Bibliographic Details
Main Authors: Adil U Rehman, Malaika Hamid, Sher Alam Khan, Muhammad Eisa, Wasim Ullah, Zia Ur Rehman, Muzammil Ahmad Khan, Sulman Basit, Noor Muhammad, Saadullah Khan, Naveed Wasif
Format: Article
Language:English
Published: MDPI AG 2022-12-01
Series:Genes
Subjects:
autosomal recessive
stuttering
exome sequencing
splice site variant
<i>ARMC3</i>
Online Access:https://www.mdpi.com/2073-4425/13/12/2299

Internet

https://www.mdpi.com/2073-4425/13/12/2299

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