Response to Letter to the Editor: "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline"

Phyllis W. Speiser, Richard J. Auchus, Deborah P. Merke, Walter L. Miller, Perrin C White

Research output: Contribution to journalArticle

Original languageEnglish (US)
Number of pages1
JournalThe Journal of clinical endocrinology and metabolism
Volume104
Issue number6
DOIs
StatePublished - Jun 1 2019

Fingerprint

Steroid 21-Hydroxylase
Practice Guidelines
Congenital adrenal hyperplasia due to 21 hydroxylase deficiency

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry
  • Endocrinology
  • Clinical Biochemistry
  • Biochemistry, medical

Cite this

Response to Letter to the Editor : "Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society Clinical Practice Guideline". / Speiser, Phyllis W.; Auchus, Richard J.; Merke, Deborah P.; Miller, Walter L.; White, Perrin C.

In: The Journal of clinical endocrinology and metabolism, Vol. 104, No. 6, 01.06.2019.

Research output: Contribution to journalArticle

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