A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation

• Misako Kunii

• Hiroshi Doi

• Yuichi Higashiyama

Journal

• Journal of human genetics / Japan Society of Human Genetics

  Journal of human genetics / Japan Society of Human Genetics 60 (4), 187-191, 2015-04

  Tokyo : Springer Nature

Details

• CRID: 1520291854802082304
• NII Article ID: 40020433141
• NII Book ID: AA11206160
• ISSN: 14345161
• NDL BIB ID: 026332543
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I026332543
• Web Site: https://search.jamas.or.jp/link/ui/2016001946
• Text Lang: en
• NDL Source Classification:
  • ZS16(科学技術--医学--人類遺伝学)
• Data Source:
  • NDL
  • CiNii Articles