Gradual Loss of ACTH Due to a Novel Mutation in LHX4: Comprehensive Mutation Screening in Japanese Patients with Congenital Hypopituitarism

• Masaki Takagi,

  Affiliations Department of Pediatrics, Keio University School of Medicine Tokyo, Japan, Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan

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• Tomohiro Ishii,

  Affiliation Department of Pediatrics, Keio University School of Medicine Tokyo, Japan

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• Mikako Inokuchi,

  Affiliation Department of Pediatrics, Keio University School of Medicine Tokyo, Japan

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• Naoko Amano,

  Affiliation Department of Pediatrics, Keio University School of Medicine Tokyo, Japan

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• Satoshi Narumi,

  Affiliation Department of Pediatrics, Keio University School of Medicine Tokyo, Japan

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• Yumi Asakura,

  Affiliation Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Kanagawa, Japan

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• Koji Muroya,

  Affiliation Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Kanagawa, Japan

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• Yukihiro Hasegawa,

  Affiliation Department of Endocrinology and Metabolism, Tokyo Metropolitan Children's Medical Center, Tokyo, Japan

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• Masanori Adachi,

  Affiliation Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Kanagawa, Japan

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• Tomonobu Hasegawa

  * E-mail: thaseg@a6.keio.jp

  Affiliation Department of Pediatrics, Keio University School of Medicine Tokyo, Japan

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