A novel deletion mutation in P2RY5/LPA6 gene cause autosomal recessive woolly hair with hypotrichosis
Author:
Publisher
Wiley
Subject
Infectious Diseases,Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-3083.2009.03514.x/fullpdf
Reference10 articles.
1. Disruption of P2RY5, an orphan G protein-coupled receptor, underlies autosomal recessive woolly hair;Shimomura;Nat Genet,2008
2. Genome-wide linkage analysis of an autosomal recessive hypotrichosis identifies a novel P2RY5 mutation;Petukhova;Genomics,2008
3. Mutations in the lipase H gene underlie autosomal recessive woolly hair/hypotrichosis;Shimomura;J Invest Dermatol,2009
4. Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in the P2RY5 gene;Shimomura;Exp Dermatol,2009
5. Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair;Horev;J Am Acad Dermatol,2009
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