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ArticleEuropean journal of human genetics : EJHG2026

A homozygote mutation in RPA2 associated with bone marrow failure, immunodeficiency, and telomere biology disorder.

Amos J Simon et al.PubMed ↗Full text ↗Publisher ↗

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3 papers cite it

2026
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Full record →Abstract, authors, funding and every citing paper · PMID 41703052