De novo COX2 mutation in a LHON family of Caucasian origin: implication for the role of mtDNA polymorphism in human pathology

• Sergey I. Zhadanov

• Vasiliy V. Atamanov

• Nikolay I. Zhadanov

Bibliographic Information

Other Title

• De novo COX2 mutation in a LHON family of Caucasian origin implication for the role of mtDNA polymorphism in human pathology

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 (3), 161-170, 2006

  Tokyo : Springer Nature

Keywords

• Leber's hereditary optic neuropathy
• Haplogroup marker
• mtDNA polymorphism
• Mitochondriopathy

Details

• CRID: 1523669555352509056
• NII Article ID: 10018115453
• NII Book ID: AA11206160
• ISSN: 14345161
• NDL BIB ID: 7838749
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I7838749
• Web Site: https://search.jamas.or.jp/link/ui/2007051241
• Text Lang: en
• NDL Source Classification:
  • ZS16(科学技術--医学--人類遺伝学)
• Data Source:
  • NDL
  • CiNii Articles