← Evidence map

ReviewEuropean journal of human genetics : EJHG2026

Strømme syndrome: the clinical and molecular spectrum associated with variants in CENPF.

Meghan R Mulligan et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

1 paper cites it

2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 42471516