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This page is a summary of: 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, October 2008, Endocrine Society,
DOI: 10.1210/jc.2008-0958.
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