ArticleGenes & diseases2020
Clinical phenotype of a Chinese patient with RIPK1 deficiency due to novel mutation.
Li Lin et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
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ArticleGenes & diseases2020
Li Lin et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.