Higher G allele frequency of RET C2307t>G polymorphism in female patients with Hirschsprung disease in Yogyakarta, Indonesia
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...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Indonesian Pediatric Society Publishing House
2008-05-01
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| Series: | Paediatrica Indonesiana |
| Subjects: | |
| Online Access: | https://paediatricaindonesiana.org/index.php/paediatrica-indonesiana/article/view/484 |