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ArticleCells2025

Exome Study of Single Nucleotide Variations in Patients with Syndromic and Non-Syndromic Autism Reveals Potential Candidate Genes for Diagnostics and Novel Single Nucleotide Variants.

Lyudmila Belenska-Todorova et al.PubMed ↗Full text ↗Publisher ↗

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3 papers cite it

2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 40558542