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17,20-Lyase Deficiency, Isolated
Known as:
17-Alpha-Hydroxylase-17,20-Lyase Deficiency, Combined Complete
, 17-ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED PARTIAL
, 17-Alpha-Hydroxylase-17,20-Lyase Deficiency, Combined Partial
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (2)
Congenital adrenal hyperplasia
Cytochrome P450
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
1994
1994
Genomic Analysis of Two Siblings with 17α-Hydroxylase Deficiency and Hypertension
Eiji Kaneko
,
Yasushi Kobayashi
,
Y. Yasukochi
,
Y. Kishi
,
F. Numano
1994
Corpus ID: 84397150
17α-hydroxylase/17, 20-lyase deficiency is an autosomal recessive disorder, which causes mineralcorticoid hypertension. Here we…
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