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ArticleClinical genetics2025

Exome Sequencing of Consanguineous Pashtun Families With Familial Epilepsy Reveals Causative and Candidate Variants in TSEN54, MOCS2, and OPHN1.

Afrasiab Khan et al.PubMed ↗Full text ↗Publisher ↗

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2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 39400946