Association of SLC26A4 muations with clinical features and thyroid function in deaf infants with enlarged vestibular aqueduct

• Satoshi Iwasaki

• Koji Tsukamoto

• Shinichi Usami

Abstract

コレクション : 国立国会図書館デジタルコレクション > デジタル化資料 > 雑誌

Journal

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 51 (9), 805-810, 2006

  Tokyo : Springer Nature

Keywords

• Deafness
• Pendred syndrome
• SLC26A4
• Thyroid
• Thyroglobulin

Details

• CRID: 1522543654690778880
• NII Article ID: 10018765653
• NII Book ID: AA11206160
• ISSN: 14345161
• NDL BIB ID: 8057606
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I8057606
• Web Site: https://search.jamas.or.jp/link/ui/2007073127
• Text Lang: en
• NDL Source Classification:
  • ZS16(科学技術--医学--人類遺伝学)
• Data Source:
  • NDL
  • CiNii Articles