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

De Novo Occurrence of the Filaggrin Mutation p.R501X with Prevalent Mutation c.3321delA in a Japanese Family with Ichthyosis Vulgaris Complicated by Atopic Dermatitis

15 Nov 2007

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 Allergic Rhinitis and Sensitization
Share to Contact Dermatitis and Allergies
Share to Dermatology and Skin Diseases

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 18007582
DOI: 10.1038/sj.jid.5701164

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

De Novo Occurrence of the Filaggrin Mutation p.R501X with Prevalent Mutation c.3321delA in a Japanese Family with Ichthyosis Vulgaris Complicated by Atopic DermatitisPMID 18007582Read ↗

Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis.Semantic proximity Read ↗

A new filaggrin gene mutation in a Korean patient with ichthyosis vulgaris.Semantic proximity Read ↗

Filaggrin Gene Mutation c.3321delA is Associated with Dry Phenotypes of Atopic Dermatitis in the Chinese Han Population.Semantic proximity Read ↗

Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris.Semantic proximity Read ↗

Increased Prevalence of Filaggrin Deficiency in 51 Patients with Recessive X-Linked Ichthyosis Presenting for Dermatological Examination.Semantic proximity Read ↗

Ichthyosis vulgaris: the filaggrin mutation disease.Semantic proximity Read ↗

An Analysis of the Filaggrin Gene Polymorphism in Korean Atopic Dermatitis Patients.Semantic proximity Read ↗

FLG mutations in ichthyosis vulgaris and atopic eczema: spectrum of mutations and population genetics.Semantic proximity Read ↗

[Filaggrin gene mutations are frequent and increase the risk of skin disease].Semantic proximity Read ↗

Filaggrin mutations and the skin.Semantic proximity Read ↗

Associations of FLG mutations between ichthyosis vulgaris and atopic dermatitis in Han Chinese.Semantic proximity Read ↗

Filaggrin haploinsufficiency among patients with dermatitis from a tertiary referral centre: early findings and possible phenotype.Semantic proximity Read ↗

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