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

Author:

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

Publication:

Cell

Publisher:

Elsevier

Date:

16 May 2003

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