Title : Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency.

Pub. Date : 1991 Aug 25

PMID : 1714904






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Steroid 17 alpha-hydroxylase deficiency is caused by defects in cytochrome P450c17, the single enzyme that has 17-alpha hydroxylase and 17,20-lyase activities. Steroids cytochrome P450 family 17 subfamily A member 1 Homo sapiens