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Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1
Prokudin, Ivan, Simons, Cas, Grigg, John R, Storen, Rebecca, Kumar, Vikrant, Phua, Zai Y, Smith, James, Flaherty, Maree, Davila, Sonia, Jamieson, Robyn VVolume:
22
Langue:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2013.268
Date:
July, 2014
Fichier:
PDF, 648 KB
english, 2014