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Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing
Timal, S., Hoischen, A., Lehle, L., Adamowicz, M., Huijben, K., Sykut-Cegielska, J., Paprocka, J., Jamroz, E., van Spronsen, F. J., Korner, C., Gilissen, C., Rodenburg, R. J., Eidhof, I., Van den HeuvVolume:
21
Langue:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/dds123
Date:
October, 2012
Fichier:
PDF, 318 KB
english, 2012