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Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis

Schrauwen, Isabelle; Valgaeren, Hanne; Tomas-Roca, Laura; Sommen, Manou; Altunoglu, Umut; Wesdorp, Mieke; Beyens, Matthias; Fransen, Erik; Nasir, Abdul; Vandeweyer, Geert; Schepers, Anne; Rahmoun, Malika; van Beusekom, Ellen; Huentelman, Matt J.; Offeciers, Erwin; Dhooghe, Ingeborg; Huber, Alex; Van de Heyning, Paul; Zanetti, Diego; De Leenheer, Els M. R.; De Leenheer, Els M. R.


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  <dc:creator>Schrauwen, Isabelle</dc:creator>
  <dc:creator>Valgaeren, Hanne</dc:creator>
  <dc:creator>Tomas-Roca, Laura</dc:creator>
  <dc:creator>Sommen, Manou</dc:creator>
  <dc:creator>Altunoglu, Umut</dc:creator>
  <dc:creator>Wesdorp, Mieke</dc:creator>
  <dc:creator>Beyens, Matthias</dc:creator>
  <dc:creator>Fransen, Erik</dc:creator>
  <dc:creator>Nasir, Abdul</dc:creator>
  <dc:creator>Vandeweyer, Geert</dc:creator>
  <dc:creator>Schepers, Anne</dc:creator>
  <dc:creator>Rahmoun, Malika</dc:creator>
  <dc:creator>van Beusekom, Ellen</dc:creator>
  <dc:creator>Huentelman, Matt J.</dc:creator>
  <dc:creator>Offeciers, Erwin</dc:creator>
  <dc:creator>Dhooghe, Ingeborg</dc:creator>
  <dc:creator>Huber, Alex</dc:creator>
  <dc:creator>Van de Heyning, Paul</dc:creator>
  <dc:creator>Zanetti, Diego</dc:creator>
  <dc:creator>De Leenheer, Els M. R.</dc:creator>
  <dc:creator>De Leenheer, Els M. R.</dc:creator>
  <dc:date>2019-01-01</dc:date>
  <dc:description>Purpose: To characterize new molecular factors implicated in a hereditary congenital facial paresis (HCFP) family and otosclerosis.</dc:description>
  <dc:identifier>https://aperta.ulakbim.gov.trrecord/70275</dc:identifier>
  <dc:identifier>oai:zenodo.org:70275</dc:identifier>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>http://www.opendefinition.org/licenses/cc-by</dc:rights>
  <dc:source>GENETICS IN MEDICINE 21(5) 1199-1208</dc:source>
  <dc:title>Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis</dc:title>
  <dc:type>info:eu-repo/semantics/article</dc:type>
  <dc:type>publication-article</dc:type>
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