<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Czell D</dc:creator>
  <dc:creator>Andersen PM</dc:creator>
  <dc:creator>Neuwirth C</dc:creator>
  <dc:creator>Morita M</dc:creator>
  <dc:creator>Weber M</dc:creator>
  <dc:date>2013</dc:date>
  <dc:identifier>https://sonar.ch/global/documents/528</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3109/21678421.2012.756525</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/23282279</dc:relation>
  <dc:source>Amyotrophic lateral sclerosis &amp; frontotemporal degeneration. - 2013</dc:source>
  <dc:subject xmlns:ns0="xml" ns0:lang="en">Amyotrophic Lateral Sclerosis</dc:subject>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Aphasia</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Male</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Middle Aged</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Mutation</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Transcription Factor TFIIIA</dc:subject>
  <dc:title xmlns:ns7="xml" ns7:lang="en">Progressive aphasia as the presenting symptom in a patient with amyotrophic lateral sclerosis with a novel mutation in the OPTN gene.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>