NDLI: Makorin ring finger 3 gene analysis in Koreans with familial precocious puberty

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Makorin ring finger 3 gene analysis in Koreans with familial precocious puberty

Content Provider	Scilit
Author	Jeong, Hwal Rim Lee, Hae Sang Hwang, Jin Soon
Copyright Year	2017
Abstract	Background: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 (Objective:To identifyMethods:26 patients with CPP and their parents (total 13 families) were recruited. We measured endocrine and auxological parameters, and sequenced allResults:We found noConclusions:mutation is uncommon in Korean patients with familial CPP. Ethnic variation in the
Related Links	http://www.degruyter.com/downloadpdf/j/jpem.2017.30.issue-11/jpem-2016-0471/jpem-2016-0471.xml
Ending Page	1201
Page Count	5
Starting Page	1197
ISSN	21910251
DOI	10.1515/jpem-2016-0471
Journal	Journal of Pediatric Endocrinology and Metabolism
Issue Number	11
Volume Number	30
Language	English
Publisher	Walter de Gruyter GmbH
Publisher Date	2017-01-01
Access Restriction	Open
Subject Keyword	Journal of Pediatric Endocrinology and Metabolism Medical Laboratory Technology Rheumatology Familial Precocious Puberty Mkrn3 Gene Polymorphism Precocious Puberty Journal: Journal of Pediatric Endocrinology and Metabolism, Issue- 4
Content Type	Text
Resource Type	Article
Subject	Endocrinology, Diabetes and Metabolism Endocrinology Pediatrics, Perinatology and Child Health

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