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Novel NPHS1 Gene Mutation in an Iranian Patient with Congenital Nephrotic Syndrome of the Finnish Type
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: 20132514
Original language: English
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