Title : A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiency.

Pub. Date : 2006 Jun

PMID : 16569739






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 The position of arginine at codon 96 was modeled using the CYP17 structure 2c17 (www.rcsb.org). Arginine cytochrome P450 family 17 subfamily A member 1 Homo sapiens