Functional study of a novel single deletion in the TITF1/NKX2.1 homeobox gene that produces congenital hypothyroidism and benign chorea but not pulmonary distress

• MOYA CM

収録刊行物

• J Clin Endocrinol Metab

  J Clin Endocrinol Metab 91 1832-1841, 2006

詳細情報

• CRID: 1572261550504586368
• NII論文ID: 10021265961
• データソース種別:
  • CiNii Articles