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ArticleMolecular biology reports2025

Novel heterozygous mutation in KMT2B causing an unusual phenotypic presentation: a comprehensive clinical and bioinformatic analysis.

Farzaneh Iravani et al.PubMed ↗Publisher ↗

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1 paper cites it

2025
2026
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Full record →Abstract, authors, funding and every citing paper · PMID 41222778