Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy

• Nagasamy Soumittra

• Sampath K Loganathan

• Dharanija Madhavan

収録刊行物

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 59 (8), 444-453, 2014-08

  Tokyo : Springer Nature

詳細情報

• CRID: 1520010380347222144
• NII論文ID: 40020171705
• NII書誌ID: AA11206160
• ISSN: 14345161
• NDL書誌ID: 025732070
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I025732070
• Web Site: https://search.jamas.or.jp/link/ui/2015145507
• 本文言語コード: en
• NDL 雑誌分類:
  • ZS16(科学技術--医学--人類遺伝学)
• データソース種別:
  • NDL
  • CiNii Articles