Novel NPHS1 Gene Mutation in an Iranian Patient with Congenital Nephrotic Syndrome of the Finnish Type

作者:Ameli Sonbol*; Zenker Martin; Zare Shahabadi Ameneh; Esfahani Seyed Taher; Madani Abbas; Monajemzadeh Maryam; Bazargani Behnaz; Ataei Nematollah; Hajezadeh Niloofar; Rezaei Nima
来源:Nefrologia, 2013, 33(5): 747-749.
DOI:10.3265/Nefrologia.pre2013.Jun.11838