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 Shim;

gynecological endocrinology 2012 Vol. 28 pp. 573-576

157

shim2012gynecologicalhomozygouscyp17a1mutation

congenital adrenal hyperplasia cyp17a1 mutations h373l japanese and chinese homozygous cyp17a1

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115195

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10.3109/09513590.2011.650743

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