Partially disturbed lamellar granule secretion in mild congenital ichthyosiform erythroderma with ALOX12B mutations
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2010.09745.x/fullpdf
Reference18 articles.
1. An update on molecular aspects of the non-syndromic ichthyoses;Akiyama;Exp Dermatol,2008
2. Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1;Jobard;Hum Mol Genet,2002
3. Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B;Eckl;J Invest Dermatol,2009
4. Autosomal recessive congenital ichthyosis;Fischer;J Invest Dermatol,2009
5. The hepoxilin connection in the epidermis;Brash;FEBS J,2007
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