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

MLA

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.” Molecular Genetics & Genomic Medicine, vol. 8, no. 9, Sept. 2020, pp. 1–10. EBSCOhost, https://doi.org/10.1002/mgg3.1167.

APA

Staretz, C. O., Schlotawa, L., Wormser, O., Golan, T. I., Birk, O. S., Ferreira, C. R., Dierks, T., & Radhakrishnan, K. (2020). A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency. Molecular Genetics & Genomic Medicine, 8(9), 1–10. https://doi.org/10.1002/mgg3.1167

Chicago

Staretz, Chacham, Orna, Lars Schlotawa, Ohad Wormser, Tripto, Inbal Golan, Ohad S. Birk, Carlos R. Ferreira, Thomas Dierks, and Karthikeyan Radhakrishnan. 2020. “A Homozygous Missense Variant of SUMF1 in the Bedouin Population Extends the Clinical Spectrum in Ultrarare Neonatal Multiple Sulfatase Deficiency.” Molecular Genetics & Genomic Medicine 8 (9): 1–10. doi:10.1002/mgg3.1167.