From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG)-Reference-Cited by-同舟云学术

From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG)

Published:2012-02-11 Issue:2 Volume:18 Page:187-196
ISSN:1382-4147
Container-title:Heart Failure Reviews
language:en
Short-container-title:Heart Fail Rev

Author:

Kapusta Livia,Zucker Nili,Frenckel George,Medalion Benjamin,Gal Tuvia Ben,Birk Einat,Mandel Hanna,Nasser Nadim,Morgenstern Sarah,Zuckermann Andreas,Lefeber Dirk J.,de Brouwer Arjen,Wevers Ron A.,Lorber Avraham,Morava Eva

Publisher

Springer Science and Business Media LLC

Subject

Cardiology and Cardiovascular Medicine

Link

http://link.springer.com/content/pdf/10.1007/s10741-012-9302-6

Reference28 articles.

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2. Jaeken J, Hennet T, Matthijs G, Freeze HH (2009) CDG nomenclature: Time for a change! Biochimica et Biophysica Acta-Molecular Basis of Disease 1792:825–826

3. Cantagrel V, Lefeber DJ, Ng BG, Guan Z, Silhavy JL, Bielas SL et al (2010) SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder. Cell 142:203–217

4. Wopereis S, Lefeber DJ, Morava E, Wevers RA (2006) Mechanisms in protein O-glycan biosynthesis and clinical and molecular aspects of protein O-glycan biosynthesis defects: a review. Clin Chem 52:574–600

5. Iijima K, Murakami F, Nakamura K, Ikawa S, Yuasa I, Motosumi H et al (1994) Hemostatic studies in patients with carbohydrate-deficient glycoprotein syndrome. Thromb Res 76:193–198

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