A carregar...

Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19.

Congenital nephrotic syndrome of the Finnish type (CNF) is an autosomal recessive disease that is characterized by massive proteinuria and nephrotic syndrome at birth. CNF represents a unique, apparently specific dysfunction of the renal basement membranes, and the estimated incidence of CNF in the...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Kestilä, M., Männikkö, M., Holmberg, C., Gyapay, G., Weissenbach, J., Savolainen, E. R., Peltonen, L., Tryggvason, K.
Formato: Artigo
Idioma:Inglês
Publicado em: 1994
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918269/
https://ncbi.nlm.nih.gov/pubmed/8178817
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!