Genetic variants of transferrin in the diagnosis of protein hypoglycosylation

Journal of Inherited Metabolic Disease

Volumn 28, Issue 6, 2005, Pages 1184-1188

  Albahri, Z ^a,b   Marklova E ^a   Vanicek H ^a   Minxova L ^a   Dedek P ^a   Skalova S ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

^b UNIVERSITY HOSPITAL HRADEC KRALOVE   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSFERRIN;

ARTICLE; CHILD; CONGENITAL DISORDER OF GLYCOSYLATION; CONTROLLED STUDY; DISEASE ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; IMMUNOLOGICAL PROCEDURES; INCIDENCE; ISOELECTRIC FOCUSING; MAJOR CLINICAL STUDY; PHENOTYPE; PROTEIN ANALYSIS; PROTEIN GLYCOSYLATION; PROTEIN HYPOGLYCOSYLATION;

ADOLESCENT; ALLELES; GLYCOSYLATION; HUMANS; HYDROGEN-ION CONCENTRATION; INFANT, NEWBORN; ISOELECTRIC FOCUSING; MALE; PHENOTYPE; POLYMORPHISM, GENETIC; PROTEIN ISOFORMS; TRANSFERRIN; VARIATION (GENETICS);

EID: 31644447885     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-005-0113-y     Document Type: Article

References (10)

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