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

Mee-Hwa Lee,Seok Won Park,Tae Ki Yoon,Sung Han Shim;Mee-Hwa Lee;Seok Won Park;Tae Ki Yoon;Sung Han S...

2012 gynecological endocrinology DOI: 10.3109/09513590.201... 143 views

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congenital adrenal hyperplasia cyp17a1 mutations h373l homozygous cyp17a1