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An Entity of Type : owl:Thing, within Data Space : data.idref.fr associated with source document(s)

AttributesValues
Author
Bibliographic Citation
  • Boycott Kym M., Beaulieu Chandree L., Kernohan Kristin D., Gebril Ola H., Mhanni Aziz, Chudley Albert E., Redl David, Qin Wen, Hampson Sarah, Kury Sebastien, Tetreault Martine, Puffenberger Erik G., Scott James N., Bezieau Stephane, Reis Andre, Uebe Steffen, Schumacher Johannes, Hegele Robert A., McLeod D. Ross, Galvez-Peralta Marina, Majewski Jacek, RAMAEKERS Vincent, Nebert Daniel W., Innes A. Micheil, Parboosingh Jillian S., Abou Jamra Rami. Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.. 2015
dc:date
  • 2015-12-03
Digital Object Identifier (DOI)
  • 10.1016/j.ajhg.2015.11.002
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