← Evidence map

ArticleMolecular genetics & genomic medicine2020

A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency.

Orna Staretz-Chacham et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

2 papers cite it

2020
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 32048457