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

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Bibliographic Details
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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