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Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease

Autosomal recessive polycystic kidney disease (ARPKD) is a rare monogenic disease with a severe phenotype often presenting prenatally or in early childhood. With its obligate renal and hepatic involvement, ARPKD is one of the most important indications for liver and/or kidney transplantation in chil...

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Bibliografische gegevens
Gepubliceerd in:Front Pediatr
Hoofdauteurs: Ebner, Kathrin, Schaefer, Franz, Liebau, Max Christoph
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Frontiers Media S.A. 2017
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC5327862/
https://ncbi.nlm.nih.gov/pubmed/28296980
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fped.2017.00018
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