Heterozygosity for the common LCHAD mutation (1528g>C) is not a major cause of HELLP syndrome and the prevalence of the mutation in the Dutch population is low

• DEN BOER ME

収録刊行物

• Pediatr Res

  Pediatr Res 48 (2), 151-154, 2000

詳細情報

• CRID: 1573950400840067072
• NII論文ID: 30027175681
• DOI: 10.1203/00006450-200008000-00006
• データソース種別:
  • CiNii Articles