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

Prenatal diagnosis of epidermolytic palmoplantar keratoderma caused by c.T470C (p.M157T) of the keratin 9 gene in a Chinese kindred.

Prenatal diagnosis - 1 Sept 2009

Chen X-L, Xu C-M, Cai S-R, Chen C-Y, Zhang X-N

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 Amino Acid Substitution
Share to Asian People
Share to DNA Mutational Analysis
Share to Methionine

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Point Mutation

Share to Pregnancy

Share to Prenatal Diagnosis

Share to Threonine

Source

Identifiers

PMID: 19548225
DOI: 10.1002/pd.2315

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal diagnosis of epidermolytic palmoplantar keratoderma caused by c.T470C (p.M157T) of the keratin 9 gene in a Chinese kindred.PMID 19548225Read ↗

Novel N160I mutation of keratin 9 in a large pedigree from Hungary with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

KRT9 gene mutation as a reliable indicator in the prenatal molecular diagnosis of epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

A novel mutation of keratin 9 in a large Chinese family with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

[Present status of the molecular genetics in epidermolytic palmoplantar keratoderma].Semantic proximity Read ↗

De novo mutation of keratin 9 gene in two Taiwanese patients with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

Possible anticipation in familial epidermolytic palmoplantar keratoderma with the p.R163W mutation of Keratin 9.Semantic proximity Read ↗

A keratin 9 Gene mutation (Asn160Ser) in a Japanese patient with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

[Mutation analysis of keratin 9 gene in a family with epidermolytic palmoplantar keratoderma].Semantic proximity Read ↗

The common KRT9 gene mutation in a Japanese patient with epidermolytic palmoplantar keratoderma and knuckle pad-like keratoses.Semantic proximity Read ↗

Mutations in the keratin 9 gene in Pakistani families with epidermolytic palmoplantar keratoderma.Semantic proximity Read ↗

[Mutation analysis of keratin 9 gene in a pedigree with epidermolytic palmoplantar keratoderma].Semantic proximity Read ↗

Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12?q21Semantic proximity Read ↗

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