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Watfa Al-Mamari

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Case report Open access Jul 2026

Clinical Phenotypes Associated with NRXN1 Deletions in Five Children with Autism Spectrum Disorder in Oman

Clinical heterogeneity among children with NRXN1 deletions illustrates clinical heterogeneity among children with autism spectrum disorder and supports the need for larger studies to better define genotype-phenotype relationships.

Samira Said AlHousni, A. Idris, Watfa Al-Mamari et al. · 0 citations