Multiple sulfatase deficiency in a Turkish family resulting from a novel mutation

Regulation of Wnt Signaling and Embryo Patterning by an Extracellular Sulfatase

Gurtej K. Dhoot, Marcus K. Gustafsson, Xingbin Ai et al. · Science · 2001 · 463 citations · Full text

Life Sciences, Developmental Biology, Molecular Biology +17

Multiple Sulfatase Deficiency Is Caused by Mutations in the Gene Encoding the Human Cα-Formylglycine Generating Enzyme

Thomas Dierks, Bernhard Schmidt, Ljudmila Borissenko et al. · Cell · 2003 · 390 citations · Full text

Life Sciences, Biochemistry, Genetics +14

The Multiple Sulfatase Deficiency Gene Encodes an Essential and Limiting Factor for the Activity of Sulfatases

Maria Pia Cosma, Stefano Pepe, Ida Annunziata et al. · Cell · 2003 · 364 citations · Full text

Life Sciences, Biochemistry, Genetics +14

A novel amino acid modification in sulfatases that is defective in multiple sulfatase deficiency

Bernhard Schmidt, Thorsten Selmer, Arnd Ingendoh et al. · Cell · 1995 · 357 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +14

Molecular and functional analysis ofSUMF1 mutations in multiple sulfatase deficiency

Maria Pia Cosma, Stefano Pepe, Giancarlo Parenti et al. · Human Mutation · 2004 · 73 citations

Life Sciences, Genetics, Molecular Genetics +16