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

Hutchinson-Gilford progeria syndrome: report of 2 cases and a novel LMNA mutation of HGPS in China.

Journal of the American Academy of Dermatology - 1 Oct 2013

Zhang Hui, Chen Xilan, Guo Yifeng, Liang Jianying, Tang Li, Yu Hong, Yao Zhirong

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 Biopsy, Needle
Share to China
Share to DNA Mutational Analysis
Share to Immunohistochemistry

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Lamin Type A

Share to Progeria

Share to Rare Diseases

Source

Identifiers

PMID: 24034385
DOI: 10.1016/j.jaad.2011.07.002

Genes

LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hutchinson-Gilford progeria syndrome: report of 2 cases and a novel LMNA mutation of HGPS in China.PMID 24034385Read ↗

LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome.Semantic proximity Read ↗

Hutchinson-Gilford progeria syndrome caused by an LMNA mutation: a case report.Semantic proximity Read ↗

Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance.Semantic proximity Read ↗

Unraveling the mysteries of Hutchinson-Gilford progeria syndrome: a comprehensive review of LMNA gene mutations.Semantic proximity Read ↗

Epidemiological characteristics of patients with Hutchinson-Gilford progeria syndrome and progeroid laminopathies in China.Semantic proximity Read ↗

p.Pro4Arg mutation in LMNA gene: a new atypical progeria phenotype without metabolism abnormalities.Semantic proximity Read ↗

[Three cases of Hutchinson-Gilford progeria syndrome].Semantic proximity Read ↗

Hutchinson-Gilford Progeria Syndrome: An Overview of the Molecular Mechanism, Pathophysiology and Therapeutic Approach.Semantic proximity Read ↗

[Analysis of a case with typical Hutchinson-Gilford progeria syndrome with scleroderma-like skin changes and review of literature].Semantic proximity Read ↗

Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy TreatmentSemantic proximity Read ↗

Hutchinson-Gilford progeria syndrome.Semantic proximity Read ↗

Hutchinson-gilford progeria syndrome and its relevance to cardiovascular diseases and normal aging.Semantic proximity Read ↗

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