Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Homozygous ARHGDIA Gene Mutation in an 11-Month-Old Infant with Steroid-Resistant Nephrotic Syndrome.

Indian journal of pediatrics - 1 Apr 2022

Narayan Aditya, Karunakar Pediredla, Krishnamurthy Sriram, Deepthi Bobbity, Jose Divakar

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Homozygote
Share to Infant
Share to Mutation
Share to Nephrotic Syndrome

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Steroids

Source

Identifiers

PMID: 35060086
DOI: 10.1007/s12098-021-04053-4

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Homozygous ARHGDIA Gene Mutation in an 11-Month-Old Infant with Steroid-Resistant Nephrotic Syndrome.PMID 35060086Read ↗

Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adultsSemantic proximity Read ↗

Nephrotic syndrome: Genetic screening in steroid-resistant nephrotic syndrome.Semantic proximity Read ↗

Novel NPHS1 Gene Mutations in two Chinese Infants with Congenital Nephrotic Syndrome.Semantic proximity Read ↗

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

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

Gene mutations and steroid-resistant nephrotic syndrome.Semantic proximity Read ↗

ANKRD11 gene deletion in a 17-year-old male.Semantic proximity Read ↗

Genetic Studies in Infants with Congenital Nephrotic Syndrome: A Case Series.Semantic proximity Read ↗

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

A novel heterozygous mutation of the NPHS1 gene in a Chinese child with congenital nephrotic syndrome: A case report.Semantic proximity Read ↗

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

A 13-Year-Old Child with Lupus-Like Nephritis and 22q11 Microduplication Syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.