1 Ocak 2014 Dergi makalesi Açık Erişim

Durlu, Yusuf K.; Koroglu, Cigdem; Tolun, Aslihan

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/61637</identifier>
  <creators>
    <creator>
      <creatorName>Durlu, Yusuf K.</creatorName>
      <givenName>Yusuf K.</givenName>
      <familyName>Durlu</familyName>
      <affiliation>Makula Eye Hlth, TR-34724 Istanbul, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Koroglu, Cigdem</creatorName>
      <givenName>Cigdem</givenName>
      <familyName>Koroglu</familyName>
      <affiliation>Bogazici Univ, Dept Mol Biol &amp; Genet, Istanbul, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Tolun, Aslihan</creatorName>
      <givenName>Aslihan</givenName>
      <familyName>Tolun</familyName>
      <affiliation>Bogazici Univ, Dept Mol Biol &amp; Genet, Istanbul, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Novel Recessive Cone-Rod Dystrophy Caused By Poc1B Mutation</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2014</publicationYear>
  <dates>
    <date dateType="Issued">2014-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/61637</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1001/jamaophthalmol.2014.1658</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
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  <descriptions>
    <description descriptionType="Abstract">IMPORTANCE A new form of cone-rod dystrophy (CORD) is described and the gene responsible for the disease is identified.</description>
  </descriptions>
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