Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F12%3A11498" target="_blank" >RIV/00216208:11110/12:11498 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11150/12:10127408 RIV/00179906:_____/12:10127408 RIV/00064165:_____/12:11498
Result on the web
<a href="http://fb.cuni.cz/file/5637/FB2012A0010.pdf" target="_blank" >http://fb.cuni.cz/file/5637/FB2012A0010.pdf</a>
DOI - Digital Object Identifier
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Result language
angličtina
Original language name
Mutational analysis of the NPHS2 gene in Czech patients with idiopathic nephrotic syndrome
Original language description
Focal segmental glomerulosclerosis and minimal change disease represent frequent histological patterns of renal injury in patients with nephrotic syndrome.
Czech name
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Czech description
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Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FE - Other fields of internal medicine
OECD FORD branch
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Project
<a href="/en/project/NS9779" target="_blank" >NS9779: Genetic factors influencing the progression of selected forms of nephrotic syndrome</a><br>
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2012
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Result description