Higher G allele frequency of RET C2307t>G polymorphism in female patients with Hirschsprung disease in Yogyakarta, Indonesia

• 主要な著者: Ahmad Hamim Sadewa (著者), Saryono Saryono (著者), Rochadi Rochadi (著者), Wiryatun Lestariana (著者), Wayan T Artama (著者)
• フォーマット: 図書
• 出版事項: Indonesian Pediatric Society Publishing House, 2008-05-01T00:00:00Z.
• 主題: article
• オンライン･アクセス: Connect to this object online.

Background Hirschsprung disease (HSCR) is a heterogenous congenital disorder and the current research show that the RET gene is a major locus involved in its pathogenesis. However, whether these genes take a part in sporadically Indonesian HSCR have not been fully understood. Objective The aim of th...