Dergi makalesi Açık Erişim
Durlu, Yusuf K.; Koroglu, Cigdem; Tolun, Aslihan
<?xml version='1.0' encoding='utf-8'?> <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>Durlu, Yusuf K.</dc:creator> <dc:creator>Koroglu, Cigdem</dc:creator> <dc:creator>Tolun, Aslihan</dc:creator> <dc:date>2014-01-01</dc:date> <dc:description>IMPORTANCE A new form of cone-rod dystrophy (CORD) is described and the gene responsible for the disease is identified.</dc:description> <dc:identifier>https://aperta.ulakbim.gov.trrecord/61637</dc:identifier> <dc:identifier>oai:zenodo.org:61637</dc:identifier> <dc:rights>info:eu-repo/semantics/openAccess</dc:rights> <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights> <dc:source>JAMA OPHTHALMOLOGY 132(10) 1185-1191</dc:source> <dc:title>Novel Recessive Cone-Rod Dystrophy Caused by POC1B Mutation</dc:title> <dc:type>info:eu-repo/semantics/article</dc:type> <dc:type>publication-article</dc:type> </oai_dc:dc>
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