Peters Plus Syndrome Is a New Congenital Disorder of Glycosylation and Involves Defective O-Glycosylation of Thrombospondin Type 1 Repeats
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference30 articles.
1. Genetic defects in the human glycome
2. Congenital Disorders of Glycosylation: A Rapidly Expanding Disease Family
3. Peters Plus Syndrome Is Caused by Mutations in B3GALTL, a Putative Glycosyltransferase
4. A novel human glycosyltransferase: primary structure and characterization of the gene and transcripts
5. The Peters’ plus syndrome: a review
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