Discover Community Create You

t/gene-rpgr

RPGR gene

Discuss publications and research concerning the RPGR gene.

0 followers0 posts21 articles

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

RPGRorf15 nanopore long-read sequencing improves retinitis pigmentosa molecular diagnosis for men and women.
RPGR
Genetics of the retina.
RPGR
Validation of Nanopore long-read sequencing to resolve RPGR ORF15 genotypes in individuals with X-linked retinitis pigmentosa.
RPGR
Female carrier of RPGR mutation presenting with high myopia.
RPGR
Clinical and analytical validation of an 82-gene comprehensive genome-profiling panel for identifying and interpreting variants responsible for inherited retinal dystrophies.
RPGR
Identification of false-negative mutations missed by next-generation sequencing in retinitis pigmentosa patients: a complementary approach to clinical genetic diagnostic testing.
RPGR
A Review of Secondary Photoreceptor Degenerations in Systemic Disease.
RPGR
Alternative splicing and retinal degeneration.
RPGR
[Clinical findings in members of a Czech family with retinitis pigmentosa caused by the c.2426_2427delAG mutation in RPGR].
RPGR
The retinitis pigmentosa GTPase regulator interacting protein 1 (RPGRIP1) links RPGR to the nephronophthisis protein network.
RPGR

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