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Abreu, A.P., Trarbach, E.B., de Castro, M., Frade-Costa, E.M., Versiani, B., Matias-Baptista, M.T., Garmes, H.M., Mendonca, B.B. and Latronico, A.C. (2008) Loss of function mutations in the genes encoding prokineticin 2 or prokineticin receptor 2 cause autosomal recessive Kallmann syndrome. The Journal of Clinical Endocrinology & Metabolism, 93, 4113-4118. doi:10.1210/jc.2008-0958

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