{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,1]],"date-time":"2025-12-01T02:24:20Z","timestamp":1764555860348,"version":"3.40.5"},"reference-count":21,"publisher":"S. Karger AG","issue":"4","license":[{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"},{"start":{"date-parts":[[2016,1,1]],"date-time":"2016-01-01T00:00:00Z","timestamp":1451606400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.karger.com\/Services\/SiteLicenses"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Sex Dev"],"published-print":{"date-parts":[[2016]]},"abstract":"<jats:p>&lt;i&gt;NR0B1&lt;\/i&gt; is the causative gene for X-linked adrenal hypoplasia congenita, characterized by adrenal insufficiency, hypogonadotropic hypogonadism, and infertility. We identified an &lt;i&gt;NR0B1 &lt;\/i&gt;frameshift mutation in a boy with precocious puberty who had no signs of adrenal insufficiency. Blood examination revealed elevated testosterone levels and gonadotropin hyperresponses to gonadotropin releasing hormone (GnRH) stimulation, together with normal adrenal hormone levels. GnRH analog treatment partially ameliorated his clinical features. Molecular analysis identified a p.Glu3fsAla*16 in &lt;i&gt;NR0B1&lt;\/i&gt;. These results expand the clinical manifestations of &lt;i&gt;NR0B1&lt;\/i&gt; mutations to include central precocious puberty without adrenal insufficiency. &lt;i&gt;NR0B1&lt;\/i&gt; mutations likely underlie androgen overproduction via GnRH-dependent and -independent mechanisms.<\/jats:p>","DOI":"10.1159\/000448726","type":"journal-article","created":{"date-parts":[[2016,9,20]],"date-time":"2016-09-20T21:02:24Z","timestamp":1474405344000},"page":"205-209","source":"Crossref","is-referenced-by-count":9,"title":["&lt;b&gt;&lt;i&gt;NR0B1&lt;\/i&gt;&lt;\/b&gt; Frameshift Mutation in a Boy with Idiopathic Central Precocious 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