Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
Tariq, M.; Ayub, M.; Jelani, M.; Basit, S.; Naz, G.; Wasif, N.; Raza, S. I.; Naveed, A. K.; Ullah Khan, S.; Azeem, Z.; Yasinzai, M.; Wali, A.; Ali, G.; Chishti, M. S.; Ahmad, W.; British Journal of Dermatology, 2009, vol. 160, issue 5, p 1006, ISSN 00070963. ISBN 13652133.

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