Corrigendum to "The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylation." Clin Chim Acta, volume 436, pages 135-139 DOI: 10.1016/j.cca.2014.05.011;The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylation

Clinica Chimica Acta

Volumn 436, Issue , 2014, Pages 135-139

  Park, Julien H ^a   Zühlsdorf, Andrea ^a   Wada, Yoshinao ^b   Roll, Claudia ^c   Rust, Stephan ^d   Du Chesne, Ingrid ^a   Grüneberg, Marianne ^a   Reunert, Janine ^a   Marquardt, Thorsten ^a  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^b OSAKA UNIVERSITY   (Japan)

^c UNIVERSITY OF WITTEN HERDECKE   (Germany)

^d Leibniz Institut für Arterioskleroseforschung   (Germany)

Author keywords

Carbohydrate deficient transferrin; Congenital disorders of glycosylation; High performance liquid chromatography; Isoelectric focusing; Mass spectrometry; Variant

Indexed keywords

ALANINE; GLUTAMIC ACID; SIALIDASE; TRANSFERRIN;

AMINO ACID SUBSTITUTION; ARTICLE; CONGENITAL DISORDER OF GLYCOSYLATION TYPE 2; CONSANGUINEOUS MARRIAGE; CONTROLLED STUDY; ELECTROSPRAY MASS SPECTROMETRY; GENE MUTATION; HETEROZYGOTE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HOMOZYGOTE; HUMAN; IMMUNOPRECIPITATION; ISOELECTRIC FOCUSING; MALE; MOLECULAR WEIGHT; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; TIME OF FLIGHT MASS SPECTROMETRY; TRANSFERRIN GENE; ARTIFACTS; BLOOD; BLOOD CHEMICAL ANALYSIS; CASE REPORT; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CONGENITAL DISORDERS OF GLYCOSYLATION; DNA MUTATIONAL ANALYSIS; FEMALE; GENETICS; HUMANS; METHODS; MUTATION; REPRODUCIBILITY OF RESULTS;

ARTIFACTS; BLOOD CHEMICAL ANALYSIS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CONGENITAL DISORDERS OF GLYCOSYLATION; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; IMMUNOPRECIPITATION; ISOELECTRIC FOCUSING; MALE; MUTATION; REPRODUCIBILITY OF RESULTS; TRANSFERRIN;

EID: 84902008723     PISSN: 00098981     EISSN: 18733492     Source Type: Journal    
DOI: 10.1016/j.cca.2015.04.001     Document Type: Erratum

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