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June 1, 1988Proceedings of the National Academy of SciencesOpen Access

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency.

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Authors

PWPerrin C. WhiteThe University of Texas Southwestern Medical CenterAVA VitekNew York Psychoanalytic Society and InstituteBDBo DupontLeiden University

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White et al. (1988) studied this question.

synapsesocial.com/papers/6a850ef2e7eca461fe847f7chttps://doi.org/10.1073/pnas.85.12.4436
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Mutation in the CYP21B gene (Ile-172----Asn) causes steroid 21-hydroxylase deficiency.1988 · 251 citations
  2. 2P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.1987 · 105 citations
  3. 3Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.1987 · 93 citations
  4. 4Congenital Adrenal Hyperplasia1987 · 123 citations