Associated Papers
Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis.
Xie Y et al.
Frontiers in Medicine, 2025
Genetic dissection of two Pakistani families with consanguineous localized autosomal recessive hypotrichosis (LAH).
Abbas S et al.
Iranian Journal of Basic Medical Sciences, 2014
A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.
Nahum S et al.
Clinical and Experimental Dermatology, 2011
Novel mutations in the P2RY5 gene in one Turkish and two Indian patients presenting with hypotrichosis and woolly hair.
Pasternack SM et al.
Archives of Dermatological Research, 2009
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
Azeem Z et al.
Human Genetics, 2008
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