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CONGENITAL NEPHROTIC SYNDROME IN AN INFANT WITH ALG1-CONGENITAL DISORDER OF GLYCOSYLATION
Congenital nephrotic syndrome in the newborn is most frequently related to mutations in genes specific for structural integrity of the glomerular basement membrane and associated filtration structures within the kidney, resulting in massive leakage of plasma proteins into the urine. Occurrence of co...
Tallennettuna:
| Julkaisussa: | Pediatr Int |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4996748/ https://ncbi.nlm.nih.gov/pubmed/27325525 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/ped.12988 |
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