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

Epidermolysis bullosa: the expanding mutation database.

The Journal of investigative dermatology - 1 Oct 2004

Uitto Jouni

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 Databases, Genetic
Share to Epidermolysis Bullosa
Share to Mutation

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15373798
DOI: 10.1111/j.0022-202X.2004.23333.x

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

Epidermolysis bullosa: the expanding mutation database.PMID 15373798Read ↗

Next-generation sequencing: comprehensive genetic testing for epidermolysis bullosa.Semantic proximity Read ↗

Genetic abnormalities and clinical classification of epidermolysis bullosaSemantic proximity Read ↗

Inherited epidermolysis bullosa: New diagnostic criteria and classificationSemantic proximity Read ↗

Revised classification system for inherited epidermolysis bullosaSemantic proximity Read ↗

Recent advances in understanding and managing epidermolysis bullosaSemantic proximity Read ↗

Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification.Semantic proximity Read ↗

Epidermolysis Bullosa. Clinical, Epidemiologic, and Laboratory Advances and the Findings of the National Epidermolysis Bullosa RegistrySemantic proximity Read ↗

Molecular diagnosis of inherited skin diseases: the paradigm of dystrophic epidermolysis bullosa.Semantic proximity Read ↗

Molecular heterogeneity of epidermolysis bullosa simplex: contribution of EXPH5 mutations.Semantic proximity Read ↗

Inherited epidermolysis bullosa: New diagnostics and new clinical phenotypes.Semantic proximity Read ↗

Recently Identified Forms of Epidermolysis BullosaSemantic proximity Read ↗

Inherited epidermolysis bullosa: recent basic and clinical advances.Semantic proximity Read ↗

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