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Nephron development and extrarenal features in a child with congenital nephrotic syndrome caused by null LAMB2 mutations
BACKGROUND: Congenital nephrotic syndrome (CNS) is a rare disorder caused by various structural and developmental defects of glomeruli. It occurs typically as an isolated kidney disorder but associates sometimes with other systemic, extrarenal manifestations. CASE PRESENTATIONS: An infant presented...
Uloženo v:
| Vydáno v: | BMC Nephrol |
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| Hlavní autoři: | , , , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2017
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5501564/ https://ncbi.nlm.nih.gov/pubmed/28683731 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-017-0632-4 |
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