<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>Sleiman MB</dc:creator>
  <dc:creator>Sleiman MB</dc:creator>
  <dc:creator>Abbas O</dc:creator>
  <dc:creator>Btadini W</dc:creator>
  <dc:creator>Najjar T</dc:creator>
  <dc:creator>Tofaili M</dc:creator>
  <dc:creator>Chedraoui A</dc:creator>
  <dc:creator>Khalil S</dc:creator>
  <dc:creator>Kibbi AG</dc:creator>
  <dc:creator>Kurban M</dc:creator>
  <dc:date>2015</dc:date>
  <dc:identifier>https://sonar.ch/global/documents/231547</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1111/1346-8138.12939</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/26046953</dc:relation>
  <dc:source>The Journal of dermatology. - 2015</dc:source>
  <dc:subject xmlns:ns0="xml" ns0:lang="en">Child</dc:subject>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Codon, Nonsense</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Hair</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Hair Diseases</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Hypotrichosis</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Lipase</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Male</dc:subject>
  <dc:title xmlns:ns8="xml" ns8:lang="en">Novel mutation in LIPH in a Lebanese patient with autosomal recessive woolly hair/hypotrichosis.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>