A novel mutation in the Lipase H gene underlies autosomal recessive hypotrichosis and woolly hair
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep00730.pdf
Reference13 articles.
1. Aslam, M. et al. A novel locus for autosomal recessive form of hypotrichosis maps to chromosome 3q26.33-q27.3. J Med Genet 41, 849–52 (2004).
2. Rafique, M. A. et al. A locus for hereditary hypotrichosis localized to human chromosome 18q21.1. Eur J Hum Genet 11, 623–8 (2003).
3. Wali, A. et al. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32. Clin Genet 72, 23–9 (2007).
4. Ali, G., Chishti, M. S., Raza, S. I., John, P. & Ahmad, W. A mutation in the lipase H (LIPH) gene underlie autosomal recessive hypotrichosis. Hum Genet 121, 319–25 (2007).
5. Inoue, A. et al. LPA-producing enzyme PA-PLAalpha regulates hair follicle development by modulating EGFR signalling. EMBO J 30, 4248–60 (2011).
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