Type I lamellar ichthyosis improved by tazarotene 0.1% gel
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2230.2003.01318.x/fullpdf
Reference10 articles.
1. Mutations of keratinocytes transglutaminase 1 in lamellar ichthyosis;Huber;Science,1995
2. Mapping of a second locus for lamellar ichthyosis to chromosome 2q33-35;Parmentier;Hum Mol Genet,1996
3. 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
4. Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2;Virolainen;Am J Hum Genet,2000
5. Mutation in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome;Lefèvre;Am J Hum Genet,2001
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