Genetic analysis of Japanese patients with 21-hydroxylase deficiency : identification of a patient with a new mutation of a homozygous deletion of adenine at codon 246 and patients without demonstrable mutations within the structural gene for CYP21

• KOYAMA S.

収録刊行物

• J. Clin. Endocrinol. Metab.

  J. Clin. Endocrinol. Metab. 87 2668-2673, 2002

詳細情報

• CRID: 1571417125584051200
• NII論文ID: 10021951360
• データソース種別:
  • CiNii Articles