A new compound heterozygous mutation in a female with 17α-hydroxylase/17,20-lyase deficiency, slipped capital femoral epiphysis, and adrenal myelolipoma

Fan YangDepartment of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, PR China; View further author information

Yongting ZhaoDepartment of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, PR China; View further author information

Jie LvDepartment of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, PR China; View further author information

Xia ShengDepartment of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, PR China; View further author information

Lihong WangDepartment of Endocrinology, The Second Affiliated Hospital of Harbin Medical University, Harbin, PR China; ;Translational Medicine Research and Cooperation Center of Northern China, Heilongjiang Academy of Medical Sciences, Harbin, ChinaCorrespondence[email protected]
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A new compound heterozygous mutation in a female with 17α-hydroxylase/17,20-lyase deficiency, slipped capital femoral epiphysis, and adrenal myelolipoma

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A new compound heterozygous mutation in a female with 17α-hydroxylase/17,20-lyase deficiency, slipped capital femoral epiphysis, and adrenal myelolipoma

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