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

Ameli, Sonbol; Esfahani, Seyed Taher; Madani, Abbas; Monajemzadeh, Maryam; Bazargani, Behnaz; Ataei, Nematollah; Hajezadeh, Niloofar; Zenker, Martin; Zare-Shahabadi, Ameneh; Rezaei, Nima.

Afiliação

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

Artigo em Inglês | IBECS | ID: ibc-117708

Biblioteca responsável: ES1.1

Localização: BNCS

RESUMEN

RESUMEN

No disponible

Assuntos

Humanos; Masculino; Lactente; Síndrome Nefrótica/congênito; Marcadores Genéticos; Biópsia; Mutação

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Texto completo: Disponível Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Biópsia / Marcadores Genéticos / Síndrome Nefrótica Limite: Humanos / Lactente / Masculino Idioma: Inglês Revista: Nefrología (Madr.) Ano de publicação: 2013 Tipo de documento: Artigo Instituição/País de afiliação: Children's Medical Center/Iran / Institute of Human Genetics/Germany / School of Medicine/s. p

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