From glycosylation disorders to dolichol biosynthesis defects: a new class of metabolic diseases
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-011-9301-0
Reference63 articles.
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4. Cantagrel V, Lefeber DJ et al. (2010) SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder. Cell 142(2):203–217
5. Carson DD, Earles BJ, et al. (1981) Enhancement of protein glycosylation in tissue slices by dolichylphosphate. J Biol Chem 256(22):11552–11557
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