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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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Auteurs principaux: Amina Mehmood, Shiza Shahzad, Hafiz Muhammad Suleman, Warda Fatima
Format: Artigo
Langue:Inglês
Publié: Elsevier 2026-01-01
Collection:In Silico Research in Biomedicine
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Accès en ligne:http://www.sciencedirect.com/science/article/pii/S3050787126003446
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