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

Expanding the Genotype of Sjögren-Larsson Syndrome: A New Case Due to Two Novel Mutations.

Actas dermo-sifiliograficas - 1 Jan 2000

García-Peris E, Latour-Álvarez I, Pestana-Eliche M, Sánchez R

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 Genotype
Share to Infant
Share to Mutation
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 28410621
DOI: 10.1016/j.ad.2016.12.015

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

Expanding the Genotype of Sjögren-Larsson Syndrome: A New Case Due to Two Novel Mutations.PMID 28410621Read ↗

Sjögren-larsson syndrome and crystalline maculopathy associated with a novel mutation.Semantic proximity Read ↗

Sjögren-Larsson syndrome caused by novel mutations in ALDH3A2 gene.Semantic proximity Read ↗

[Sjögren-Larsson syndrome].Semantic proximity Read ↗

Genetics and epigenetics of primary Sjögren syndrome: implications for future therapiesSemantic proximity Read ↗

Sjögren-Larsson syndrome due to a novel mutation in the FALDH gene.Semantic proximity Read ↗

An early view of the international Sjögren's syndrome registry.Semantic proximity Read ↗

Sjögren-Larsson syndrome in clinical practice.Semantic proximity Read ↗

A novel 4 bp deletion mutation in the FALDH gene segregating in a Turkish family with Sjögren-Larsson syndrome.Semantic proximity Read ↗

Molecular basis of Sjögren-Larsson syndrome: frequency of the 1297-1298 del GA and 943C-->T mutation in 29 patients.Semantic proximity Read ↗

Novel autoantibodies in Sjögren's syndrome: A comprehensive reviewSemantic proximity Read ↗

Four cases of hypofibrinogenemia associated with four novel mutations.Semantic proximity Read ↗

Pathogenesis of Sjögren’s syndrome: What we know and what we should learnSemantic proximity Read ↗

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