H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
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- Nagasaki Keisuke
- Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medicine and Dental Sciences
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- Usui Takeshi
- Clinical Research Institute Center for Endocrine and Metabolic Diseases, National Hospital Organization, Kyoto Medical Center
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- Asami Tadashi
- Faculty of Nursing, Social Welfare, and Psychology, Department of Nursing, Niigata Seiryo University
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- Ogawa Yohei
- Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medicine and Dental Sciences
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- Kikuchi Toru
- Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medicine and Dental Sciences
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- Uchiyama Makoto
- Division of Pediatrics, Department of Homeostatic Regulation and Development, Niigata University Graduate School of Medicine and Dental Sciences
この論文をさがす
収録刊行物
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- Clinical Pediatric Endocrinology
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Clinical Pediatric Endocrinology 18 (4), 111-113, 2009
日本小児内分泌学会
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詳細情報 詳細情報について
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- CRID
- 1390282679461691264
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- NII論文ID
- 10031199601
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- NII書誌ID
- AA11006467
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- ISSN
- 13477358
- 09185739
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- CiNii Articles
- KAKEN