postnatal growth retardation_Scn1b<tm1.1Bion>/Scn1b<tm1.1Bion>

http://metadb.riken.jp/0001732NSScn1btm11BionScn1btm11BionScn1btm11Bion

postnatal growth retardation_Scn1b<tm1.1Bion>/Scn1b<tm1.1Bion>

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 I, beta
  http://metadb.riken.jp/db/mgi_rdf/MGI:98247

遺伝子型

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

• Scn1b<tm1.1Bion>/Scn1b<tm1.1Bion>

アレルシンボル

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

• Scn1b<tm1.1Bion>

遺伝的背景

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

• Not Specified

MP annotation

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

• postnatal growth retardation
  http://purl.obolibrary.org/obo/MP_0001732

文献

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

• Verena C. Wimmer, et.al., Axon initial segment dysfunction in a mouse model of genetic epilepsy with febrile seizures plus., The Journal of clinical investigation, 2010, 120
  http://rdf.ncbi.nlm.nih.gov/pubmed/20628201