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ArticleGlobal medical genetics2024

Identification of Two Variants c.2697A > C and c.3305A > C in USP7 by Analysis of Whole-Exome Sequencing in Chinese Patients with Hao-Fountain Syndrome.

Mei Sun et al.PubMed ↗Full text ↗Publisher ↗

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1 paper cites it

2024
2025
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Full record →Abstract, authors, funding and every citing paper · PMID 38229971