CYP17A1 Intron Mutation Causing Cryptic Splicing in 17α-Hydroxylase Deficiency

• Daw-Yang Hwang,

  Affiliation Division of Nephrology, Department of Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan

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• Chi-Chih Hung,

  Affiliation Division of Nephrology, Department of Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan

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• Felix G. Riepe,

  Affiliation Division of Pediatric Endocrinology, Department of Pediatrics, Christian Albrechts University, Kiel, Germany

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• Richard J. Auchus,

  Affiliation Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan, United States of America

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• Alexandra E. Kulle,

  Affiliation Division of Pediatric Endocrinology, Department of Pediatrics, Christian Albrechts University, Kiel, Germany

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• Paul-Martin Holterhus,

  Affiliation Division of Pediatric Endocrinology, Department of Pediatrics, Christian Albrechts University, Kiel, Germany

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• Mei-Chyn Chao,

  Affiliations Division of Genetics, Endocrinology and Metabolism, Department of Pediatrics, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan, Department of Medical Genetics, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

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• Mei-Chuan Kuo,

  Affiliations Division of Nephrology, Department of Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan, Faculty of Renal Care, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

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• Shang-Jyh Hwang ,

  * E-mail: sjhwang@kmu.edu.tw

  Affiliations Division of Nephrology, Department of Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan, Faculty of Renal Care, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

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• Hung-Chun Chen

  Affiliations Division of Nephrology, Department of Medicine, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan, Faculty of Renal Care, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan

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