ArticleRMD open2016
ADA2 deficiency: case report of a new phenotype and novel mutation in two sisters.
F Uettwiller et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
28 papers cite it
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ArticleRMD open2016
F Uettwiller et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.