← Evidence map

ArticleHaematologica2023

One gene, two opposite phenotypes: a case report of hereditary anemia due to a loss-of-function variant in the

Barbara Eleni Rosato et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

1 paper cites it

2023
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 37102609