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2. A homozygous missense variant of SUMF1 in the Bedouin population extends the clinical spectrum in ultrarare neonatal multiple sulfatase deficiency. Issue 9 (12th February 2020)

4. Arylsulfatase K inactivation causes mucopolysaccharidosis due to deficient glucuronate desulfation of heparan and chondroitin sulfate. Issue 17 (17th September 2020)

10. Drug screening identifies tazarotene and bexarotene as therapeutic agents in multiple sulfatase deficiency. Issue 3 (15th February 2023)