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Article

No mutation of elastin and fibulin-5 genes in a patient with acquired cutis laxa associated with chronic urticaria.

The British journal of dermatology - 1 Jan 2011

Sun X-K, Chen J-F

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Identifiers

PMID: 20849517
DOI: 10.1111/j.1365-2133.2010.10049.x

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Related research

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No mutation of elastin and fibulin-5 genes in a patient with acquired cutis laxa associated with chronic urticaria.PMID 20849517Read ↗

Cutis laxa: a review.Semantic proximity Read ↗

A p.C217R mutation in fibulin-5 from cutis laxa patients is associated with incomplete extracellular matrix formation in a skin equivalent model.Semantic proximity Read ↗

A novel elastin gene mutation resulting in an autosomal dominant form of cutis laxa.Semantic proximity Read ↗

Cutis Laxa.Semantic proximity Read ↗

Identification of a de novo mutation of the elastin gene by targeted exome sequencing in autosomal dominant cutis laxa.Semantic proximity Read ↗

New insights into the pathogenesis of autosomal-dominant cutis laxa with report of five ELN mutations.Semantic proximity Read ↗

Autosomal recessive cutis laxa syndrome revisited.Semantic proximity Read ↗

Lethal cutis laxa with contractural arachnodactyly, overgrowth and soft tissue bleeding due to a novel homozygous fibulin-4 gene mutation.Semantic proximity Read ↗

[Mutation of the fibulin-5 gene in recessive autosomal cutis laxa].Semantic proximity Read ↗

An autosomal-recessive form of cutis laxa is due to homozygous elastin mutations, and the phenotype may be modified by a heterozygous fibulin 5 polymorphism.Semantic proximity Read ↗

Cutis laxa with pulmonary emphysema, conjunctivochalasis, nasolacrimal duct obstruction, abnormal hair, and a novel FBLN5 mutation.Semantic proximity Read ↗

Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene.Semantic proximity Read ↗

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