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Novel NPHS1 Gene Mutation in an Iranian Patient with Congenital Nephrotic Syndrome of the Finnish Type
Ameli, Sonbol; Esfahani, Seyed Taher; Madani, Abbas; Monajemzadeh, Maryam; Bazargani, Behnaz; Ataei, Nematollah; Hajezadeh, Niloofar; Zenker, Martin; Zare-Shahabadi, Ameneh; Rezaei, Nima.
Affiliation
  • Ameli, Sonbol; Children's Medical Center. Pediatrics Center of Excellence. Tehran University of Medical Sciences. Tehran. Iran
  • Esfahani, Seyed Taher; Children's Medical Center. Pediatrics Center of Excellence. Tehran University of Medical Sciences. Tehran. Iran
  • Madani, Abbas; Children's Medical Center. Pediatrics Center of Excellence. Tehran University of Medical Sciences. Tehran. Iran
  • Monajemzadeh, Maryam; Children's Medical Center. Pediatrics Center of Excellence. Tehran University of Medical Sciences. Tehran. Iran
  • Bazargani, Behnaz; Children's Medical Center. Pediatrics Center of Excellence. Tehran University of Medical Sciences. Tehran. Iran
  • Ataei, Nematollah; Children's Medical Center. Pediatrics Center of Excellence. Tehran University of Medical Sciences. Tehran. Iran
  • Hajezadeh, Niloofar; Children's Medical Center. Pediatrics Center of Excellence. Tehran University of Medical Sciences. Tehran. Iran
  • Zenker, Martin; Institute of Human Genetics. University Hospital of Magdeburg. s. c. Germany
  • Zare-Shahabadi, Ameneh; Children's Medical Center. Research Center for Immunodeficiencies. Tehran University of Medical Sciences. Tehran. Iran
  • Rezaei, Nima; School of Medicine. Department of Immunology. Children's Medical Center. s. c. s. p
Nefrología (Madr.) ; 33(5): 747-749, oct. 2013. ilus
Article in En | IBECS | ID: ibc-117708
Responsible library: ES1.1
Localization: BNCS
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Full text: 1 Collection: 06-national / ES Database: IBECS Main subject: Biopsy / Genetic Markers / Nephrotic Syndrome Limits: Humans / Infant / Male Language: En Journal: Nefrología (Madr.) Year: 2013 Document type: Article
Fulltext
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Full text: 1 Collection: 06-national / ES Database: IBECS Main subject: Biopsy / Genetic Markers / Nephrotic Syndrome Limits: Humans / Infant / Male Language: En Journal: Nefrología (Madr.) Year: 2013 Document type: Article