Case Report

A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course
  • Emine Çamtosun
  • Sarah E. Flanagan
  • Sian Ellard
  • Zeynep Şıklar
  • Khalid Hussain
  • Pınar Kocaay
  • Merih Berberoğlu
J Clin Res Pediatr Endocrinol 2015; 7: 144-147 DOI: 10.4274/jcrpe.1963 PMID:26316438

Other

HADH Mutation is a Rare Cause of Hyperinsulinaemic Hypoglycaemia
  • Elif Özsu
  • Gül Yeşiltepe Mutlu
  • Filiz Mine Çizmecioğlu
  • Şükrü Hatun
J Clin Res Pediatr Endocrinol 2015; 7: 12-12

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