[A follow-up study of 10 Uyghur children with 11β-hydroxylase deficiency in the Xinjiang region]
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Objectives: To study the clinical characteristics, treatment outcomes, and CYP11B1 gene mutation spectrum in Uyghur children with 11β-hydroxylase deficiency (11β-OHD) in Xinjiang, and to explore the ethnic-specific features of ... ...
