Wanda M. Gerding, et.al., Ccdc66 null mutation causes retinal degeneration and dysfunction., Human molecular genetics, 2011, 20

http://rdf.ncbi.nlm.nih.gov/pubmed/21680557

Wanda M. Gerding, et.al., Ccdc66 null mutation causes retinal degeneration and dysfunction., Human molecular genetics, 2011, 20

pubmed

表現型アノテーション

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

• abnormal rod electrophysiology_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0004021I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• abnormal retinal rod cell morphology_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0001005I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• abnormal photoreceptor inner segment morphology_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0003730I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• thin retinal outer nuclear layer_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0008515I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• retinal photoreceptor degeneration_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0008450I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• retinal rod cell degeneration_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0008451I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• retinal cone cell degeneration_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0008444I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• abnormal photoreceptor outer segment morphology_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0003729I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• abnormal retinal photoreceptor layer morphology_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0003728I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst
• abnormal cone electrophysiology_Ccdc66<Gt(E021F10)Wrst>/Ccdc66<Gt(E021F10)Wrst>
  http://metadb.riken.jp/0004022I129P2OlaHsdC57BL6NCcdc66GtE021F10WrstCcdc66GtE021F10WrstCcdc66GtE021F10Wrst