Staretz‐Chacham, O., Schlotawa, L., Wormser, O., Golan‐Tripto, I., Birk, O. S., Ferreira, C. R., . . . Radhakrishnan, K. (2020). A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency. Mol Genet Genomic Med.

Staretz‐Chacham, Orna, Lars Schlotawa, Ohad Wormser, Inbal Golan‐Tripto, Ohad S. Birk, Carlos R. Ferreira, Thomas Dierks, e Karthikeyan Radhakrishnan. "A Homozygous Missense Variant of SUMF1 in the Bedouin Population Extends the Clinical Spectrum in Ultrarare Neonatal Multiple Sulfatase Deficiency." Mol Genet Genomic Med 2020.

Staretz‐Chacham, Orna, et al. "A Homozygous Missense Variant of SUMF1 in the Bedouin Population Extends the Clinical Spectrum in Ultrarare Neonatal Multiple Sulfatase Deficiency." Mol Genet Genomic Med 2020.