Loss-of-function variant in spermidine/spermine N1-acetyl transferase like 1 (SATL1) gene as an underlying cause of autism spectrum disorder

Loss-of-function variant in spermidine/spermine N1-acetyl transferase like 1 (SATL1) gene as an underlying cause of autism spectrum disorder

Abstract Autism spectrum disorder (ASD) is a complicated, lifelong neurodevelopmental disorder affecting verbal and non-verbal communication and social interactions. ASD signs and symptoms appear early in development before the age of 3 years. It is unlikely for a person to acquire autism after a pe...

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Príomhchruthaitheoirí: Abdulfatah M. Alayoubi, Muhammad Iqbal, Hassan Aman, Jamil A. Hashmi, Laila Alayadhi, Khalid Al-Regaiey, Sulman Basit
Formáid: Alt
Teanga:English
Foilsithe / Cruthaithe: Nature Portfolio 2024-03-01
Sraith:Scientific Reports
Ábhair:
Late onset ASD
Polyamines
Mutation
Exome sequencing
Rochtain ar líne:https://doi.org/10.1038/s41598-024-56253-5

Ar líne

https://doi.org/10.1038/s41598-024-56253-5

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