Genetic variants of transferrin in the diagnosis of protein hypoglycosylation-Reference-Cited by-同舟云学术

Genetic variants of transferrin in the diagnosis of protein hypoglycosylation

Published:2005-12 Issue:6 Volume:28 Page:1184-1188
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Albahri Z.,Marklová E.,Vaníček H.,Minxová L.,Dédek P.,Skálová S.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://www.springerlink.com/index/pdf/10.1007/s10545-005-0113-y

Reference10 articles.

1. Albahri Z, Marklová E, Vanícek H, et al (2004) Our experience with diagnostics of congenital disorders of glycosylation. Acta Medica (Hradec Králové) 47: 269–274.

2. Bean P, Sutphin MS, Necessary P, et al (1996) Carbohydrate-deficient transferrin evaluation in dry blood spots. Alcohol Clin Exp Res 20: 56–60.

3. Jaeken J (2003) Komrower Lecture. Congenital disorders of glycosylation (CDG): It's all in it! J Inherit Metab Dis 26: 99–118.

4. Jeppsson JO, Franzen B (1982) Typing of genetic variants of alpha 1 antitrypsin by electrofocusing. Clin Chem 28: 219–225.

5. Kamboh MI, Ferrell RE (1987) Human transferrin polymorphism (review). Hum Hered 37: 65–81.

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