ArticleHuman genome variation2024
A case of severe Aicardi-Goutières syndrome with a homozygous RNASEH2B intronic variant.
Yuri Shibata et al.PubMed ↗Full text ↗Publisher ↗
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ArticleHuman genome variation2024
Yuri Shibata et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.