Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby.
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.2001.04412.x/fullpdf
Reference17 articles.
1. Keratoma hereditarium mutilans
2. A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families
3. A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome
4. Loricrin Mutation in Vohwinkel’s Keratoderma Is Unique to the Variant with Ichthyosis
5. Loricrin gene mutation in a Japanese patient of Vohwinkel's syndrome
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