Autosomal recessive woolly hair with hypotrichosis caused by a novel homozygous mutation in theP2RY5gene
Author:
Publisher
Wiley
Subject
Dermatology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0625.2008.00788.x/fullpdf
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4. Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia;Cichon;Hum Mol Genet,1998
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