1 Ocak 2016 Dergi makalesi Açık Erişim

Djemie, Tania; Weckhuysen, Sarah; von Spiczak, Sarah; Carvill, Gemma L.; Jaehn, Johanna; Anttonen, Anna-Kaisa; Brilstra, Eva; Caglayan, Hande S.; de Kovel, Carolien G.; Depienne, Christel; Gaily, Eija; Hamalainen, Eija; Giraldez, Beatriz G.; Gormley, Padhraig; Guerrero-Lopez, Rosa; Guerrini, Renzo; Hamalainen, Eija; Hartmann, Corinna; Hernandez-Hernandez, Laura; Hjalgrim, Helle; Hjalgrim, Helle

Dublin Core

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  <dc:creator>Djemie, Tania</dc:creator>
  <dc:creator>Weckhuysen, Sarah</dc:creator>
  <dc:creator>von Spiczak, Sarah</dc:creator>
  <dc:creator>Carvill, Gemma L.</dc:creator>
  <dc:creator>Jaehn, Johanna</dc:creator>
  <dc:creator>Anttonen, Anna-Kaisa</dc:creator>
  <dc:creator>Brilstra, Eva</dc:creator>
  <dc:creator>Caglayan, Hande S.</dc:creator>
  <dc:creator>de Kovel, Carolien G.</dc:creator>
  <dc:creator>Depienne, Christel</dc:creator>
  <dc:creator>Gaily, Eija</dc:creator>
  <dc:creator>Hamalainen, Eija</dc:creator>
  <dc:creator>Giraldez, Beatriz G.</dc:creator>
  <dc:creator>Gormley, Padhraig</dc:creator>
  <dc:creator>Guerrero-Lopez, Rosa</dc:creator>
  <dc:creator>Guerrini, Renzo</dc:creator>
  <dc:creator>Hamalainen, Eija</dc:creator>
  <dc:creator>Hartmann, Corinna</dc:creator>
  <dc:creator>Hernandez-Hernandez, Laura</dc:creator>
  <dc:creator>Hjalgrim, Helle</dc:creator>
  <dc:creator>Hjalgrim, Helle</dc:creator>
  <dc:date>2016-01-01</dc:date>
  <dc:description>Background</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/60339</dc:identifier>
  <dc:identifier>oai:zenodo.org:60339</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>MOLECULAR GENETICS &amp; GENOMIC MEDICINE 4(4) 457-464</dc:source>
  <dc:title>Pitfalls in genetic testing: the story of missed SCN1A mutations</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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