A complex heterozygous mutation of His373Leu and Asp487-Ser488-Phe489 deletion in human cytochrome P450c17 causes 17alpha-hydroxylase/17,20-lyase deficiency in three Chinese sisters.

Source:http://linkedlifedata.com/resource/pubmed/id/12706306

Mol. Cell. Endocrinol. 2003 Mar 28 201 1-2 189-95

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PMID
12706306