{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,22]],"date-time":"2025-12-22T18:29:38Z","timestamp":1766428178041},"reference-count":54,"publisher":"Walter de Gruyter GmbH","issue":"11","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2017,1,26]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Background:<\/jats:title><jats:p>Precocious puberty is known as an idiopathic, sporadic disease. Recently, specific mutations have been shown to cause familial central precocious puberty (CPP). The makorin ring finger 3 (<\/jats:p><\/jats:sec><jats:sec><jats:title>Objective:<\/jats:title><jats:p>To identify<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods:<\/jats:title><jats:p>26 patients with CPP and their parents (total 13 families) were recruited. We measured endocrine and auxological parameters, and sequenced all<\/jats:p><\/jats:sec><jats:sec><jats:title>Results:<\/jats:title><jats:p>We found no<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions:<\/jats:title><jats:p>mutation is uncommon in Korean patients with familial CPP. Ethnic variation in the<\/jats:p><\/jats:sec>","DOI":"10.1515\/jpem-2016-0471","type":"journal-article","created":{"date-parts":[[2017,10,8]],"date-time":"2017-10-08T10:01:15Z","timestamp":1507456875000},"source":"Crossref","is-referenced-by-count":13,"title":["Makorin ring finger 3 gene analysis in Koreans with familial precocious puberty"],"prefix":"10.1515","volume":"30","author":[{"given":"Hwal Rim","family":"Jeong","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hae Sang","family":"Lee","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jin Soon","family":"Hwang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"374","reference":[{"key":"ref441","doi-asserted-by":"crossref","first-page":"783","DOI":"10.1093\/hmg\/8.5.783","article-title":"A novel imprinted gene, encoding a RING zinc-finger protein, and overlapping antisense transcript in the Prader-Willi syndrome critical region","volume":"8","year":"1999","journal-title":"Hum Mol Genet"},{"key":"ref341","doi-asserted-by":"crossref","first-page":"10972","DOI":"10.1073\/pnas.1834399100","article-title":"Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54","volume":"100","year":"2003","journal-title":"Proc Natl Acad Sci USA"},{"key":"ref271","doi-asserted-by":"crossref","first-page":"2366","DOI":"10.1056\/NEJMcp0800459","article-title":"Clinical practice. 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