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17 alpha-hydroxylase/17,20-lyase deficiency: from clinical investigation to molecular definition.

Author(s): T Yanase, Jane M Waterman, David Simpson

Publication date: 1991-01-31

Journal: Endocrine Reviews

Keywords: Adrenal Hyperplasia, Congenital, enzymology, genetics, pathology, Aldehyde-Lyases, deficiency, Amino Acid Sequence, Base Sequence, Cytochrome P-450 Enzyme System, Humans, Molecular Sequence Data, Steroid 17-alpha-Hydroxylase

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DOI:: 10.1210/edrv-12-1-91

PubMed ID:: 2026124

ScienceOpen disciplines: Chemistry

Keywords: Adrenal Hyperplasia, Congenital,enzymology,genetics,pathology,Aldehyde-Lyases,deficiency,Amino Acid Sequence,Base Sequence,Cytochrome P-450 Enzyme System,Humans,Molecular Sequence Data,Steroid 17-alpha-Hydroxylase

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ScienceOpen disciplines: Chemistry

Keywords: Adrenal Hyperplasia, Congenital, enzymology, genetics, pathology, Aldehyde-Lyases, deficiency, Amino Acid Sequence, Base Sequence, Cytochrome P-450 Enzyme System, Humans, Molecular Sequence Data, Steroid 17-alpha-Hydroxylase

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