In silico functional, structural, and therapeutic analysis of SNPs in the human NRXN1 gene linked to autism spectrum disorder

Autism Spectrum Disorder (ASD) is the most under-addressed yet prevalent neurodevelopmental condition and it is associated with genetic variants in synaptic proteins such as Neurexin 1. This study aimed to structurally and functionally characterize deleterious missense single nucleotide polymorphism...

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Hlavní autoři:	Amina Mehmood, Shiza Shahzad, Hafiz Muhammad Suleman, Warda Fatima
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Elsevier 2026-01-01
Edice:	In Silico Research in Biomedicine
Témata:	NRXN1 protein Autism spectrum disorder SNP Phytochemicals Molecular docking Neurodevelopment
On-line přístup:	http://www.sciencedirect.com/science/article/pii/S3050787126003446
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