Carregant...
Genotype–Phenotype Correlations in Non-Finnish Congenital Nephrotic Syndrome
Mutations in NPHS1, which encodes nephrin, are the main causes of congenital nephrotic syndrome (CNS) in Finnish patients, whereas mutations in NPHS2, which encodes podocin, are typically responsible for childhood-onset steroid-resistant nephrotic syndrome in European populations. Genotype–phenotype...
Guardat en:
Autors principals: | , , , , , , , , , , |
---|---|
Format: | Artigo |
Idioma: | Inglês |
Publicat: |
American Society of Nephrology
2010
|
Matèries: | |
Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3152225/ https://ncbi.nlm.nih.gov/pubmed/20507940 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2009121309 |
Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|