Transient congenital hypothyroidism caused by biallelic mutations of the dual oxidase 2 gene in Japanese patients detected by a neonatal screening program

Journal of Clinical Endocrinology and Metabolism

Volumn 93, Issue 11, 2008, Pages 4261-4267

  Maruo, Yoshihiro ^a   Takahashi, Hiroko ^a   Soeda, Ikumi ^a   Nishikura, Noriko ^a   Matsui, Katsuyuki ^a   Ota, Yoriko ^a   Mimura, Yu ^a   Mori, Asami ^a   Sato, Hiroshi ^a   Takeuchi, Yoshihiro ^a  

^a SHIGA UNIVERSITY OF MEDICAL SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

SODIUM IODIDE SYMPORTER; THYROID HORMONE; THYROID PEROXIDASE; THYROTROPIN; THYROXINE;

ARTICLE; CHILD; CLINICAL ARTICLE; CONGENITAL HYPOTHYROIDISM; CONTROLLED STUDY; DUOX2 GENE; FEMALE; GENE; GENE FREQUENCY; GENE IDENTIFICATION; GENE MUTATION; HEALTH PROGRAM; HORMONE SUBSTITUTION; HUMAN; JAPANESE; MALE; NEWBORN; NEWBORN SCREENING; PRIORITY JOURNAL; THYROTROPIN BLOOD LEVEL; THYROXINE BLOOD LEVEL;

EID: 57349176149     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2008-0856     Document Type: Article

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