Autosomal Recessive Congenital Ichthyosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference10 articles.
1. The hepoxilin connection in the epidermis;Brash;FEBS J,2007
2. Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosis;Eckl;Hum Mutat,2005
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. Mutations of keratinocyte transglutaminase in lamellar ichthyosis;Huber;Science,1995
5. Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in nonbullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1;Jobard;Hum Mol Genet,2002
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