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Article

Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type.

Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia - 1 Jan 2013

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

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Source

Identifiers

PMID: 24089175
DOI: 10.3265/Nefrologia.pre2013.Jun.11838

Genes

NPHS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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Novel NPHS1 gene mutation in an Iranian patient with congenital nephrotic syndrome of the Finnish type.PMID 24089175Read ↗

Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome.Semantic proximity Read ↗

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NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome.Semantic proximity Read ↗

Structure of the Gene for Congenital Nephrotic Syndrome of the Finnish Type (NPHS1) and Characterization of MutationsSemantic proximity Read ↗

Novel and known nephrin gene (NPHS1) mutations in two Greek cases with congenital nephrotic syndrome including a complex genotype.Semantic proximity Read ↗

Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome.Semantic proximity Read ↗

Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.Semantic proximity Read ↗

NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome.Semantic proximity Read ↗

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Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.Semantic proximity Read ↗

Three Novel Heterozygous Mutations of NPHS1 Gene Causing Infants with Congenital Nephrotic Syndrome: Two Chinese (Han) Cases.Semantic proximity Read ↗

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