Mutational analysis of SIAT1 gene : exclusion of a positional candidate for congenital hypothyroidism

• TAKAHASHI Tsutomu

  Department of Pediatrics, Akita University School of Medicine

• 小松 真紀

  秋田大学医学部小児科

• 高田 五郎

  秋田大学医学部小児科

• PAUWS E

  Academic Medical Center, University of Amsterdam, Emma Children's Hospital AMC, Laboratory of Pediatric Endocrinology

• RIS-STALPERS C

  Academic Medical Center, University of Amsterdam, Emma Children's Hospital AMC, Laboratory of Pediatric Endocrinology

Bibliographic Information

Other Title

• 優性遺伝形式を示す甲状腺機能低下症2家系の病因解析 : ポジショナル候補遺伝子SIAT1遺伝子の解析

Journal

• ホルモンと臨牀

  ホルモンと臨牀 51 (11), 945-948, 2003-11-01

Details

• CRID: 1570009750192263424
• NII Article ID: 10012432830
• NII Book ID: AN00231838
• ISSN: 00457167
• Web Site: https://search.jamas.or.jp/link/ui/2004077094
• Text Lang: ja
• Data Source:
  • CiNii Articles