| Literature DB >> 12757700 |
Abstract
The posttranslational conversion of cysteine to C(alpha)-formylglycine in the catalytic site of mammalian sulfatases is deficient in the rare but devastating disorder multiple sulfatase deficiency (MSD). Two papers in this issue of Cell report the cloning of a gene responsible for this activity.Entities:
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Year: 2003 PMID: 12757700 DOI: 10.1016/s0092-8674(03)00354-4
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582