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Shinkuma, S., Akiyama, M., Inoue, A., Aoki, J., Natsuga, K., Nomura, T., Arita, K., Abe, R., Ito, K., Nakamura, H., Ujiie, H., Shibaki, A., Suga, H., Tsunemi, Y., Nishie, W. and Shimizu, H. (2010) Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA- PLA1alpha in autosomal recessive hypotrichosis. Human Mutation, 31, 602-610.

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