About: The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype     Goto   Sponge   NotDistinct   Permalink

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scientific journal article

AttributesValues
rdf:type
description
  • artículu científicu espublizáu en 2011 (ast)
  • наукова стаття, опублікована в жовтні 2011 (uk)
  • vědecký článek publikovaný v roce 2011 (cs)
  • 2011 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած (hyw)
  • 2011 թվականի հոտեմբերին հրատարակված գիտական հոդված (hy)
  • vedecký článok (publikovaný 2011/10/15) (sk)
  • مقالة علمية (نشرت في 15-10-2011) (ar)
  • wetenschappelijk artikel (gepubliceerd op 2011/10/15) (nl)
  • scientific journal article (en)
  • im Oktober 2011 veröffentlichter wissenschaftlicher Artikel (de)
publication date
publication date
cites work
cites work
author name string
author name string
  • Arie Struyk
  • Melissa J Spencer
  • Ekaterina Mokhonova
rdfs:label
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (en)
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (nl)
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (ast)
skos:prefLabel
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (en)
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (nl)
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (ast)
name
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (en)
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (nl)
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (ast)
author
author
title
title
  • The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype (en)
page(s)
page(s)
  • 3925-3932
instance of
instance of
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