A carregar...
Congenital Nephrotic Syndrome – Finish Type
INTRODUCTION: Identification of the NPHS1 gene, which encodes nephrin, was followed by many studies demonstrating its mutation as a frequent cause of congenital nephrotic syndrome (CNS). While this gene is found in 98% of Finnish children with this syndrome, non-Finnish cases have lower level of inc...
Na minha lista:
| Publicado no: | Med Arch |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AVICENA, d.o.o., Sarajevo
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5010061/ https://ncbi.nlm.nih.gov/pubmed/27594755 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5455/medarh.2016.70.232-234 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|