A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele

• TUSIE-LUNA M. T.

Journal

• Mol. Endocrinol.

  Mol. Endocrinol. 5 685-692, 1991

Details

• CRID: 1571417125584050176
• NII Article ID: 10021951373
• Data Source:
  • CiNii Articles