Multiple Sulfatase Deficiency Is Caused by Mutations in the Gene Encoding the Human Cα-Formylglycine Generating Enzyme-Reference-Cited by-同舟云学术

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

Published:2003-05 Issue:4 Volume:113 Page:435-444
ISSN:0092-8674
Container-title:Cell
language:en
Short-container-title:Cell

Author:

Dierks Thomas,Schmidt Bernhard,Borissenko Ljudmila V.,Peng Jianhe,Preusser Andrea,Mariappan Malaiyalam,von Figura Kurt

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference46 articles.

1. Gapped BLAST and PSI-BLAST;Altschul;Nucleic Acids Res.,1997

2. Overexpression of N-acetylgalactosamine-4-sulphatase induces a multiple sulphatase deficiency in mucopolysaccharidosis-type-VI fibroblasts;Anson;Biochem. J.,1993

3. Vectors for efficient expression in mammalian fibroblastoid, myeloid and lymphoid cells via transfection or infection;Artelt;Gene,1988

4. Studies in metachromatic leukodystrophy. XII. Multiple sulfatase deficiency;Austin;Arch. Neurol.,1973

5. Multiple deficiency of mucopolysaccharide sulfatases in mucosulfatidosis;Basner;Pediatr. Res.,1979

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