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Article

Evidence for genetic modifiers other than filaggrin mutations in X-linked ichthyosis.

Journal of dermatological science - 1 Apr 2010

Gruber Robert, Janecke Andreas R, Grabher Daniela, Sandilands Aileen, Fauth Christine, Schmuth Matthias

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PMID: 20149601
DOI: 10.1016/j.jdermsci.2010.01.002

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Related research

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Evidence for genetic modifiers other than filaggrin mutations in X-linked ichthyosis.PMID 20149601Read ↗

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

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

Filaggrin mutations and the skin.Semantic proximity Read ↗

Filaggrin mutations are genetic modifying factors exacerbating X-linked ichthyosis.Semantic proximity Read ↗

Filaggrin loss-of-function mutations and association with allergic diseases.Semantic proximity Read ↗

Variants in the Gene Encoding Filaggrin Cause Autosomal-Dominant Symmetrical Acral Keratoderma.Semantic proximity Read ↗

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

Filaggrin mutations associated with skin and allergic diseases.Semantic proximity Read ↗

Exacerbation of X-linked ichthyosis phenotype in a female by inheritance of filaggrin and steroid sulfatase mutations.Semantic proximity Read ↗

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

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

Filaggrin mutations are associated with ichthyosis vulgaris in the Bangladeshi population.Semantic proximity Read ↗

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