HomozygousCYP17A1mutation (H373L) identified in a 46,XX female with combined 17α-hydroxylase/17,20-lyase deficiency

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ID: 115195
2012
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shim2012gynecologicalhomozygouscyp17a1mutation Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Mee-Hwa Lee,Seok Won Park,Tae Ki Yoon,Sung Han Shim;Mee-Hwa Lee;Seok Won Park;Tae Ki Yoon;Sung Han Shim;
Journal gynecological endocrinology
Year 2012
DOI
10.3109/09513590.2011.650743
URL
https://sciprofiles.com/publication/view/11818c248961c9645d485f870027bc73
Keywords
congenital adrenal hyperplasia cyp17a1 mutations h373l japanese and chinese homozygous cyp17a1

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