Transferrin D Protein Variants in the Diagnosis of Congenital Disorders of Glycosylation (CDG)
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F09%3A00201745" target="_blank" >RIV/00179906:_____/09:00201745 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11150/09:00208760
Result on the web
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DOI - Digital Object Identifier
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Alternative languages
Result language
angličtina
Original language name
Transferrin D Protein Variants in the Diagnosis of Congenital Disorders of Glycosylation (CDG)
Original language description
This paper discusses an analytical problem in the differentiation between congenital disorders of glycosylation (CDG; transferrin as a marker of hypoglycosylation) and transferrin protein variants, namely the type D.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FG - Paediatrics
OECD FORD branch
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Result continuities
Project
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Continuities
Z - Vyzkumny zamer (s odkazem do CEZ)
Others
Publication year
2009
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of Clinical Laboratory Analysis
ISSN
0887-8013
e-ISSN
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Volume of the periodical
23
Issue of the periodical within the volume
2
Country of publishing house
US - UNITED STATES
Number of pages
5
Pages from-to
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UT code for WoS article
000264665000002
EID of the result in the Scopus database
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