Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type

Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type

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Main Authors: Ameli,Sonbol, Zenker,Martin, Zare-Shahabadi,Ameneh, Taher Esfahani,Seyed, Madani,Abbas, Monajemzadeh,Maryam, Bazargani,Behnaz, Ataei,Nematollah, Hajezadeh,Niloofar, Rezaei,Nima
Format: Digital revista
Language:English
Published: Sociedad Española de Nefrología 2013
Online Access:http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952013000600023
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spelling oai:scielo:S0211-699520130006000232013-11-07Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish typeAmeli,SonbolZenker,MartinZare-Shahabadi,AmenehTaher Esfahani,SeyedMadani,AbbasMonajemzadeh,MaryamBazargani,BehnazAtaei,NematollahHajezadeh,NiloofarRezaei,NimaSociedad Española de NefrologíaNefrología (Madrid) v.33 n.5 20132013-01-01journal articletext/htmlhttp://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952013000600023en
institution SCIELO
collection OJS
country España
countrycode ES
component Revista
access En linea
databasecode rev-scielo-es
tag revista
region Europa del Sur
libraryname SciELO
language English
format Digital
author Ameli,Sonbol
Zenker,Martin
Zare-Shahabadi,Ameneh
Taher Esfahani,Seyed
Madani,Abbas
Monajemzadeh,Maryam
Bazargani,Behnaz
Ataei,Nematollah
Hajezadeh,Niloofar
Rezaei,Nima
spellingShingle Ameli,Sonbol
Zenker,Martin
Zare-Shahabadi,Ameneh
Taher Esfahani,Seyed
Madani,Abbas
Monajemzadeh,Maryam
Bazargani,Behnaz
Ataei,Nematollah
Hajezadeh,Niloofar
Rezaei,Nima
Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type
author_facet Ameli,Sonbol
Zenker,Martin
Zare-Shahabadi,Ameneh
Taher Esfahani,Seyed
Madani,Abbas
Monajemzadeh,Maryam
Bazargani,Behnaz
Ataei,Nematollah
Hajezadeh,Niloofar
Rezaei,Nima
author_sort Ameli,Sonbol
title Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type
title_short Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type
title_full Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type
title_fullStr Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type
title_full_unstemmed Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type
title_sort novel nphs1 gene mutation in an iranian patient with congenital nephrotic syndrome of the finnish type
publisher Sociedad Española de Nefrología
publishDate 2013
url http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952013000600023
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