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

Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?

30 Nov 2011

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 Cytomegalovirus and herpesvirus research
Share to Retinal Development and Disorders
Share to RNA regulation and disease

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 22126752
DOI: 10.1038/ejhg.2011.217

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Intellectual disability associated with retinal dystrophy in the Xp11.3 deletion syndrome: ZNF674 on trial. Guilty or innocent?PMID 22126752Read ↗

The genetic landscape of intellectual disability arising from chromosome X.Semantic proximity Read ↗

Unveiling ZNF124 as a novel determinant in neurodegeneration: orchestration of photoreceptor homeostasis through MSX2 transcriptional regulation.Semantic proximity Read ↗

ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.Semantic proximity Read ↗

Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation.Semantic proximity Read ↗

A Hidden Structural Variation in a Known IRD Gene: A Cautionary Tale of Two New Disease Candidate GenesSemantic proximity Read ↗

Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy.Semantic proximity Read ↗

X-linked mental retardation: many genes for a complex disorder.Semantic proximity Read ↗

What's in a name? RPGR mutations redefine the genetic and phenotypic landscape in retinal degenerative diseases.Semantic proximity Read ↗

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