muscular atrophy_Scn8a<med>/Scn8a<med>

http://metadb.riken.jp/0002269PCTScn8amedScn8amedScn8amed

muscular atrophy_Scn8a<med>/Scn8a<med>

表現型アノテーション

MGI marker

http://metadb.riken.jp/db/mgi_rdf/variant_of

• sodium channel, voltage-gated, type VIII, alpha
  http://metadb.riken.jp/db/mgi_rdf/MGI:103169

遺伝子型

http://metadb.riken.jp/db/mgi_rdf/allele_composition

• Scn8a<med>/Scn8a<med>

アレルシンボル

http://metadb.riken.jp/db/mgi_rdf/allele_symbol

• Scn8a<med>

遺伝的背景

http://metadb.riken.jp/db/mgi_rdf/genetic_background

• PCT

MP annotation

http://metadb.riken.jp/db/bioresource_schema/brs_indicatesPhenotype

• muscular atrophy
  http://purl.obolibrary.org/obo/MP_0002269

文献

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

• L W. Duchen, Hereditary motor end-plate disease in the mouse: light and electron microscopic studies., Journal of neurology, neurosurgery, and psychiatry, 1970, 33
  http://rdf.ncbi.nlm.nih.gov/pubmed/4315332