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

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Sonbol Amelia, Martin Zenkerb, Ameneh Zare-shahabadic, Seyed Taher Esfahania, Abbas Madania, Maryam Monajemzadeha, Behnaz Bazargania, Nematollah Ataeia, Niloofar Hajezadeha, Nima Rezaeid

a Tehran University of Medical Sciences, Pediatrics Center of Excellence, Children's Medical Center, Tehran, Iran,

b University Hospital of Magdeburg, Institute of Human Genetics, Magdeburg, Germany,

c Tehran University of Medical Sciences, Research Center for Immunodeficiencies, Children's Medical Center, Tehran, Iran,

d Tehran University of Medical Sciences, Research Center for Immunodeficiencies, Children's Medical Center; and Department of Immunology, School of Medicine, Tehran, Iran,

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ISSN: 02116995
Original language: English

DOI:10.3265/Nefrologia.pre2013.Jun.11838

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