Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome - Abreu, Ana Paula; Trarbach, Ericka Barbosa; Castro, Margaret de; Costa, Elaine Maria Frade; Versiani, Beatriz; Baptista, Maria Tereza Matias; Garmes, Heraldo Mendes; Mendonça, Berenice Bilharinho; Latronico, Ana Claudia (Journal of Clinical Endocrinology and Metabolism, 2008)