Ramakrishna. Kurapati, et.al., Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb., Human molecular genetics, 2012, 21

http://rdf.ncbi.nlm.nih.gov/pubmed/22199023

Ramakrishna. Kurapati, et.al., Myofibrillar myopathy caused by a mutation in the motor domain of mouse MyHC IIb., Human molecular genetics, 2012, 21

pubmed

allele

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

• Myh4<arl>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4839531

表現型アノテーション

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

• skeletal muscle fiber degeneration_Myh4<arl>/Myh4<arl>
  http://metadb.riken.jp/0009412IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl
• centrally nucleated skeletal muscle fibers_Myh4<arl>/Myh4<arl>
  http://metadb.riken.jp/0009404IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl
• increased variability of skeletal muscle fiber size_Myh4<arl>/Myh4<arl>
  http://metadb.riken.jp/0009403IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl
• hindlimb paralysis_Myh4<arl>/Myh4<arl>
  http://metadb.riken.jp/0000755IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl
• myositis_Myh4<arl>/Myh4<arl>
  http://metadb.riken.jp/0004510IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl
• abnormal skeletal muscle fiber morphology_Myh4<arl>/Myh4<arl>
  http://metadb.riken.jp/0003084IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl
• muscular atrophy_Myh4<arl>/Myh4<arl>
  http://metadb.riken.jp/0002269IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl
• abnormal gait_Myh4<arl>/Myh4<arl>
  http://metadb.riken.jp/0001406IC3HHeHC57BL6JMyh4arlMyh4arlMyh4arl

class

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

• Myh4<arl>
  http://metadb.riken.jp/db/mgi_rdf/MGI:4839531