Discover Community Create You

t/gene-nphs1

NPHS1 gene

Discuss publications and research concerning the NPHS1 gene.

0 followers0 posts17 articles

Create Post

TitleDiscussionLink a PMID (optional)

All posts discussion question review note

Create the first post

Ask a question, share an idea or link scientific evidence.

Topic rules

Follow Noodle’s community and scientific integrity rules.

Moderators

Managed by the Noodle moderation team.

Related literature

Exploratory whole-exome sequencing identifies candidate DNA variants in Ocular Behcet disease: a pilot study from a Pakistani cohort.
NPHS1
Novel NPHS1 Gene Mutations in two Chinese Infants with Congenital Nephrotic Syndrome.
NPHS1
Congenital nephrotic syndrome with a novel NPHS1 mutation.
NPHS1
Novel NPHS1 gene mutations in a Chinese family with congenital nephrotic syndrome.
NPHS1
Functional analysis of NPHS1 mutations in Japanese patients.
NPHS1
[Changing c.106delG (p.Ala36fs*6) loss syndrome associated with congenital Finnish type: first case diagnosed in Togo].
NPHS1
Does NPHS1 polymorphism modulate P118l mutation in NPHS2?
NPHS1
Mutations in NPHS1 in a Chinese child with congenital nephrotic syndrome.
NPHS1
Expanding the clinical spectrum of congenital nephrotic syndrome caused by NPHS1 mutations.
NPHS1
Expanding the spectrum of NPHS1-associated disease.
NPHS1

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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