A novel compound heterozygous mutation of K494_V495 deletion plus R496L and D487_F489 deletion in extreme C-terminus of cytochrome P450c17 causes 17alpha-hydroxylase deficiency

Please use this identifier to cite or link to this item: http://ir.sinica.edu.tw/handle/201000000A/7580

Title:	A novel compound heterozygous mutation of K494_V495 deletion plus R496L and D487_F489 deletion in extreme C-terminus of cytochrome P450c17 causes 17alpha-hydroxylase deficiency
Authors:	Lee, L. S. Shu, W. J. Wu, C. M. Hsieh, C. H. Chen, S. M. Hu, C. J. Chen, W. Y. Chung, B. C.
Issue Date:	2006
Relation:	Mol Cell Endocrinol 249, 16-20
URI:	http://ir.sinica.edu.tw/handle/201000000A/7580
ISSN:	http://gateway.isiknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=Drexel&SrcApp=hagerty_opac&KeyRecord=0303-7207&DestApp=JCR&RQ=IF_CAT_BOXPLOT
URL:	http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=16483711
Appears in Collections:	分子生物研究所

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