Title : Molecular basis of 17α-hydroxylase/17,20-lyase deficiency.

Pub. Date : 1992 Dec

PMID : 22217842






2 Functional Relationships(s)
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1 Based on the results obtained so far we can predict that those 17alpha-hydroxylase deficient individuals having a homozygous stop codon in the CYP17 gene positioned at the amino terminal side of the P450c17 heme-binding cysteine (442) will all have the same phenotype. Heme cytochrome P450 family 17 subfamily A member 1 Homo sapiens
2 Based on the results obtained so far we can predict that those 17alpha-hydroxylase deficient individuals having a homozygous stop codon in the CYP17 gene positioned at the amino terminal side of the P450c17 heme-binding cysteine (442) will all have the same phenotype. Heme cytochrome P450 family 17 subfamily A member 1 Homo sapiens