Bo. Chang, et.al., A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene., Proceedings of the National Academy of Sciences of the United States of America, 2009, 106

http://rdf.ncbi.nlm.nih.gov/pubmed/19887631

Bo. Chang, et.al., A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene., Proceedings of the National Academy of Sciences of the United States of America, 2009, 106

pubmed

表現型アノテーション

http://purl.org/net/cito/citesAsAuthority

• retinal cone cell degeneration_Pde6c<cpfl1>/Pde6c<cpfl1>
  http://metadb.riken.jp/0008444B6CXB1Pde6ccpfl1Pde6ccpfl1Pde6ccpfl1Pde6ccpfl1
• decreased retinal cone cell number_Pde6c<cpfl1>/Pde6c<cpfl1>
  http://metadb.riken.jp/0008446B6CXB1Pde6ccpfl1Pde6ccpfl1Pde6ccpfl1Pde6ccpfl1
• abnormal retinal inner nuclear layer morphology_Pde6c<cpfl1>/Pde6c<cpfl1>
  http://metadb.riken.jp/0003733B6CXB1Pde6ccpfl1Pde6ccpfl1Pde6ccpfl1Pde6ccpfl1

トランスクリプトームデータ

http://rdf.ncbi.nlm.nih.gov/pubmed/

• CD40910
  http://metadb.riken.jp/db/BrainTx/TranscriptomeData/CD40910