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Monnier, C., Dode, C., Fabre, L., Teixeira, L., Labesse, G., Pin, J.P., Hardelin, J.P. and Rondard, P. (2009) PROKR2 missense mutations associated with Kallmann syndrome impair receptor signaling activity. Human Molecular Genetics, 18, 75-81. doi:10.1093/hmg/ddn318

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