Sjögren-Larsson syndrome in Brazil is caused by a common c.1108-1G→C splice-site mutation in the ALDH3A2 gene
Author:
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.2006.07135.x/fullpdf
Reference8 articles.
1. The molecular basis of Sjögren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase gene;Rizzo;Am J Hum Genet,1999
2. Sjögren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2);Rizzo;Hum Mutat,2005
3. Sjögren-Larsson syndrome: biochemical defects and follow up in three cases;Auada;Eur J Dermatol,2002
4. Human liver fatty aldehyde dehydrogenase: microsomal localization, purification, and biochemical characterization;Kelson;Biochim Biophys Acta,1997
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