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

[Current advances in gene diagnosis and therapy of gelatinous drop-like corneal dystrophy].

Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences - 1 Mar 2006

Huo Ya-nan, Yao Yu-feng

Abstract excerpt

Gelatinous drop-like corneal dystrophy (GDLD) is an autosomal recessive hereditary disease, which may result in bilateral loss of vision. The gene responsible for GDLD, M1S1 is mapped on the short arm of chromosome 1 (1p), but the possible etiology of this disease remains unclear. Corneal transpl...

Read the complete abstract on PubMed

Topics

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

Share to Antigens, Neoplasm
Share to Cell Adhesion Molecules
Share to Chromosomes, Human, Pair 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Corneal Dystrophies, Hereditary

Share to DNA Mutational Analysis

Share to Epithelial Cell Adhesion Molecule

Share to Mutation

Source

Identifiers

PMID: 16610095
DOI: 10.3785/j.issn.1008-9292.2006.02.022

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16610095-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Current advances in gene diagnosis and therapy of gelatinous drop-like corneal dystrophy].PMID 16610095Read ↗

Identification of the gene responsible for gelatinous drop-like corneal dystrophy.Semantic proximity Read ↗

Road to a Genetic Model of Gelatinous Drop-Like Corneal Dystrophy.Semantic proximity Read ↗

Gelatinous drop-like corneal dystrophy: a review.Semantic proximity Read ↗

A spectrum of clinical manifestations of gelatinous drop-like corneal dystrophy in japan.Semantic proximity Read ↗

Allelic and locus heterogeneity in autosomal recessive gelatinous drop-like corneal dystrophy.Semantic proximity Read ↗

Clinical and basic aspects of gelatinous drop-like corneal dystrophy.Semantic proximity Read ↗

Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy.Semantic proximity Read ↗

Corneal dystrophies in Japan.Semantic proximity Read ↗

Two brothers with gelatinous drop-like dystrophy at different stages of the disease: role of mutational analysis.Semantic proximity Read ↗

Gelatinous drop-like corneal dystrophy.Semantic proximity Read ↗

Phenotypic investigation of cell junction-related proteins in gelatinous drop-like corneal dystrophy.Semantic proximity Read ↗

A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy.Semantic proximity Read ↗

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